Synthesis of Polysubstituted 3-Aminothiophenes from Thioamides and

Subscriber access provided by UNIV OF DURHAM

Note

Synthesis of polysubstituted 3-aminothiophenes from thioamides and allenes via tandem thio-Michael addition/oxidative annulation and 1,2-sulfur migration Teng Han, Yu Wang, Hong-Liang Li, Xiaoyan Luo, and Wei-Ping Deng J. Org. Chem., Just Accepted Manuscript • DOI: 10.1021/acs.joc.7b02616 • Publication Date (Web): 28 Dec 2017 Downloaded from http://pubs.acs.org on December 28, 2017

Just Accepted “Just Accepted” manuscripts have been peer-reviewed and accepted for publication. They are posted online prior to technical editing, formatting for publication and author proofing. The American Chemical Society provides “Just Accepted” as a free service to the research community to expedite the dissemination of scientific material as soon as possible after acceptance. “Just Accepted” manuscripts appear in full in PDF format accompanied by an HTML abstract. “Just Accepted” manuscripts have been fully peer reviewed, but should not be considered the official version of record. They are accessible to all readers and citable by the Digital Object Identifier (DOI®). “Just Accepted” is an optional service offered to authors. Therefore, the “Just Accepted” Web site may not include all articles that will be published in the journal. After a manuscript is technically edited and formatted, it will be removed from the “Just Accepted” Web site and published as an ASAP article. Note that technical editing may introduce minor changes to the manuscript text and/or graphics which could affect content, and all legal disclaimers and ethical guidelines that apply to the journal pertain. ACS cannot be held responsible for errors or consequences arising from the use of information contained in these “Just Accepted” manuscripts.

The Journal of Organic Chemistry is published by the American Chemical Society. 1155 Sixteenth Street N.W., Washington, DC 20036 Published by American Chemical Society. Copyright © American Chemical Society. However, no copyright claim is made to original U.S. Government works, or works produced by employees of any Commonwealth realm Crown government in the course of their duties.

Page 1 of 17 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

The Journal of Organic Chemistry

Synthesis thioamides

of

polysubstituted and

allenes

via

3-aminothiophenes tandem

from

thio-Michael

addition/oxidative annulation and 1,2-sulfur migration Teng Han, Yu Wang, Hong-Liang Li, Xiaoyan Luo* and Wei-Ping Deng* School of Pharmacy and Shanghai Key Laboratory of New Drug Design, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China

ABSTRACT: A facile synthetic method for the construction of 3-aminothiophenes from readily available thioamides and alllenes in the presence of a TBAI/TBHP catalyst system was developed. This protocol represents an efficient and straightforward way to access highly functionalized thiophenes in moderate to excellent yields under mild conditions, via a tandem thio-Michael addition, oxidative annulation and 1,2-sulfur migration pathway. Thiophene is a core structure found in a variety of pharmaceutical molecules, natural products and functional materials.1 It also serves as valuable building blocks in synthetic chemistry.2 Therefore, considerable efforts have been devoted to developing highly efficient and straightforward synthetic methods to access this privileged heterocyclic core.3 According to the literature, the synthetic methods can be classified to two general strategies, one is the direct functionalization of simple thiophenes,4 the other is the cyclization of the suitable sulfur-containing fragments.5,6 Recently, sulfur-containing compounds β-ketothioamides, due to its versatile reactivity properties,7 have been extensively employed for the synthesis of 2-

ACS Paragon Plus Environment

The Journal of Organic Chemistry 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 2 of 17

aminothiophene derivatives.8 We also demonstrated two novel protocols for the synthesis of polysubstituted 2-aminothiophene by treating different electrophiles DDQ and 2-ynals with βketothioamides.9 However, the present methods, to the best of our knowledge, were mainly centered on the synthesis of 2-aminothiophenes. Therefore, the development of a convenient and straightforward methodology for the synthesis of 3-aminothiophenes, in view of their biological activities of 3-aminothiophenes (Figure. 1), is still highly desired.

Figure 1. Selected pharmaceutical molecules and bioactive structure bearing highly substituted thiophene. On the other hand, allene derivatives are important and versatile building blocks in synthetic chemistry, and have been widely used for constructing structurally diverse heterocycles.10,11 We recently described a direct α, β-double electrophilic reaction by the treatment of allene-1,3dicarboxylic esters with 1,3-dicarbonyl compounds or enamines under a mild KI/tert-butyl hydroperoxide (TBHP) reaction system to construct the multi-substituted furans and pyrroles respectively (Scheme 1a).12 With the continuing interests in developing novel method for the synthesis of structurally diverse and potentially biological active heterocycles,9

,12

We further

envisaged whether a new combination of allene-1,3-dicarboxylic ester and thioamide would generate polysubstituted thiophene skeleton via the similar α, β-double electrophilic reaction


Page 3 of 17 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


mode as our previous reports. Herein, we would like to demonstrate an efficient synthetic protocol for the construction of 3-aminothiophene skeleton by the reaction of allenes with βketothioamides in the presence of a TBAI/TBHP system, through an unexpected 1,2-sulfur migration pathway (Scheme 1b).

Scheme 1. The strategies for synthesis of structurally diverse heterocycles. Our investigation began with the reaction of N, N-dimethyl-3-oxobutanethioamide (1a) and dimethyl penta-2,3-dienedioate (2a) in the presence of KI and TBHP in 1,4-dioxane at room temperature. To our delight, the reaction proceeded smoothly, however affording a 3aminothiophene product 3aa in 71% yield instead of desired 2-aminothiophene product (Table 1, Entry 1). This unexpected result may suggest a novel synthetic strategy for constructing 3aminothiophene (Scheme 1b). Encouraged by this finding, we further optimized the reaction conditions. Firstly, a variety of iodine sources such as TBAI, I2, NaI were examined (Table 1, Entries 2–4). It was found that TBAI was the most efficient catalyst in this reaction (Table 1, Entry 2). Moreover, other oxidants were evaluated and we found that TBHP was the best choice (Table 1, Entries 5−7). Additionally, the solvent effect was also investigated and 1,4-dioxane was



Page 4 of 17

found to be the optimal solvent (Table 1, Entries 8−12). Further optimization by adjusting the molar ratio of the substrates 1a and 2a showed that 1.5 equiv. of 2a was optimal to afford the desired product 3aa in 85% yield (Table 1, Entries 13-14). Therefore, the combination of 1a (1.0 equiv.), 2a (1.5 equiv.) in the presence of 20 mol% TBAI and 2 equiv. TBHP in 1,4-dioxane at room temperature was determined as the optimal reaction conditions, providing 3aa in 85% yield (Table 1, Entry 13). Table 1. Optimization of reaction conditionsa

Cat.

[O]

Solvent

Yield [%]b

1

KI

TBHP

1,4-dioxane

71

2

TBAI

TBHP

1,4-dioxane

84

entry

3

I2

TBHP

1,4-dioxane

72

4

NaI

TBHP

1,4-dioxane

72

5

TBAI

TBPB

1,4-dioxane

36

6

TBAI

DTBP

1,4-dioxane

29

7

TBAI

H2O2

1,4-dioxane

40

8

TBAI

TBHP

THF

82

9

TBAI

TBHP

EtOAc

79

10

TBAI

TBHP

CH3CN

61

11

TBAI

TBHP

diethyl ether

54

12

TBAI

TBHP

EtOH

72

13c

TBAI

TBHP

1,4-dioxane

85

d

TBAI TBHP 1,4-dioxane 82 14 Reaction conditions: 1a (0.2 mmol), 2a (0.2 mmol), Cat. (0.04 mmol), oxidant (0.4 mmol), solvent (1 mL), under air atmosphere, 6h. b Isolated yield. c 1a (0.2 mmol), 2a (0.3 mmol). d 1a (0.3 mmol), 2a (0.2 mmol). 6h.

a

Under the optimal conditions, substrate scope of this synthetic protocol was investigated (Scheme 2). Firstly, the reaction was extended to a variety of different substituted thioamides 1. The results revealed that various alkyl or phenyl substituted thioamides 1 all reacted smoothly


Page 5 of 17 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


with allenes and gave corresponding multi-substituted 3-aminothiophene structure in moderate to good yields (Scheme 2 3aa-3da). It is worth mentioning that the thioamide 1e with electron donating phenyl group gave the product 3ea in 75% yield, while the substrate 1f with electronwithdrawing phenyl group afforded 3fa in only moderate yield (47%). Furthermore, malonatederived thioamides all reacted smoothly with dimethyl penta-2,3-dienedioate (2a) to afford 3ga−3ja in good yields (74−87%). The N, N-dimethyl thioamide motif can be replaced by other amino groups and also afford corresponding 3ka-3oa in moderate to good yields. The structure of compound 3la was determined by single-crystal X-ray diffraction analysis (see the Supporting Information). Notably, the 3-(dimethylamino)-N, N-dimethyl-3-thioxopropanamide can also be transformed into the corresponding 3-aminothiophene 3pa in 78% yield. Moreover, when the ethyl ester-substituted allene was employed instead of methyl ester had no significant effect on the yield of the reaction and the desired product (3gb) was obtained in 84% yield.



Scheme 2. Scope of thioamides. Reaction conditions: 1 (0.2 mmol), 2a, 2b (0.3mmol), TBAI (0.04 mmol), TBHP (0.4 mmol), 1,4-dioxane (1 mL). Isolated yield, 6h. To account for the reaction process, a hypothetic mechanism was proposed based on literature reports and our previous work (Scheme 3).7b, 12 Initially, β-ketothioamides 1 reacts with allenes to give thio-Michael addition product A, which is followed by intermolecular nucleophilic ringclosing reaction to give key four-membered ring intermediate B. Further iodination of intermediate B undergoes via two different pathways, affording intermediate C and C’ through iodination of carbonyl α-carbon (path a) 13 or iodination of sulfur 14, respectively. Intermediate C is further subjected to an unprecedented ring-expanding process through a 1,2-sulfur migration to form intermediate D. Alternatively, the intermediate C’ undergoes an intramolecular nucleophilic attack process to give intermediate D. Finally, the intermediate D undergoes an isomerization process to give the 1,2-sulfur migration product 3.

Scheme 3. A plausible mechanism. CONCLUSION In summary, we have successfully developed an efficient TBAI-catalyzed synthesis of polysubstituted thiophenes via a tandem thio-Michael addition/oxidative annulation and 1,2sulfur migration from readily available thioamides and allenes. This protocol features mild reaction conditions, broad substrate scope, and represents a novel synthetic strategy for the


Page 6 of 17

Page 7 of 17 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


construction of 3-aminothiophenes, which would be of great importance for the drug discovery in terms of the structure diversity of thiophene derivatives. EXPERIMENTAL SECTION General Information Commercial reagents were used without further purification, unless otherwise noted. Melting points were obtained in open capillary tubes using a micromelting point apparatus which was uncorrected. The mass spectra were recorded on a TOF mass spectrometer using the EI method. 1

H NMR was recorded using 400M spectrometer at ambient temperatures and the CDCl3 as the

solvent. Chemical shifts (in ppm) with internal TMS signal is 0.0 ppm as standard are reported as (s= singlet, d= doublet, t= triplet, q= quartet, and m= multiplet).13C NMR spectra were recorded on a 100 MHz spectrometer by broadband spin decoupling for CDCl3 at ambient temperatures. The standard of chemical shifts (in ppm) is the signal of internal chloroform which at 77.16 ppm. TLC was performed by using commercially prepared 100–400 mesh silica gel plates, and visualization was effected at 254 or 365 nm. General procedure for the preparation of polysubstituted thiophenes (3aa-3gb). Thioamides compounds 1 (0.2 mmol), allene 2 (0.3mmol), and TBHP (0.4 mmol) were added to a solution of TBAI (0.04 mmol) in dry 1,4-dioxane (1 mL) under an air atmosphere. The mixture was then stirred at room temperature until the reaction was nearly completed monitored by the TLC. The resulting mixture was concentrated in vacuum and then purified by column chromatography on 100–200 mesh silica gel to afford the desired products 3. The Preparation of β-ketothioamides 1 is based on references.15



Methyl

Page 8 of 17

4-(dimethylamino)-2-(2-methoxy-2-oxoethyl)-5-propionylthiophene-3-carboxylate

(3aa) Yellow oil, 50.8 mg, 85% yield; 1H NMR (400 MHz, CDCl3) δ 3.91 (s, 2H), 3.88 (s, 3H), 3.73 (s, 3H), 2.87 (s, 6H), 2.53 (s, 3H). 13C NMR (100 MHz, CDCl3) δ 189.5, 169.5, 164.5, 154.9, 145.5, 128.9, 128.3, 52.6, 52.1, 43.9, 35.8, 28.9. HRMS (EI) calcd for C13H17NO5S [M]＋: 299.0822, found: 299.0828. Methyl

5-(dimethylamino)-3-(2-methoxy-2-oxoethyl)-4-propionylthiophene-2-

carboxylate (3ba) Yellow oil, 53.8 mg, 86% yield; 1H NMR (400 MHz, CDCl3) δ 3.90 (s, 2H), 3.87 (s, 3H), 3.73 (s, 3H), 2.92 – 2.87 (m, 2H), 2.87 (s, 6H), 1.19 (t, J = 7.4 Hz, 3H).

13

C NMR (100

MHz, CDCl3) δ 192.5, 169.6, 164.6, 154.7, 144.8, 128.8, 126.9, 52.6, 52.2, 43.8, 35.8, 34.6, 8.8. HRMS (EI) calcd for C14H19NO5S [M]+: 313.0978, found: 313.0982. Methyl

4-(dimethylamino)-2-(2-methoxy-2-oxoethyl)-5-pivaloylthiophene-3-

carboxylate (3ca) Yellow oil, 48.4 mg, 71% yield; 1H NMR (400 MHz, CDCl3) δ 3.90 (s, 2H), 3.87 (s, 3H), 3.73 (s, 3H), 2.75 (s, 6H), 1.34 (s, 9H).

13

C NMR (100 MHz, CDCl3) δ 200.3, 169.8,

164.6, 155.9, 141.6, 127.5, 118.9, 52.6, 52.1, 44.8, 43.7, 35.5, 28.1. HRMS (EI) calcd for C16H23NO5S [M]+: 341.1291, found: 341.1296. Methyl

5-benzoyl-4-(dimethylamino)-2-(2-methoxy-2-oxoethyl)

(3da)


thiophene-3-carboxylate

Page 9 of 17 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


Yellow oil, 39.7 mg, 55% yield; 1H NMR (400 MHz, CDCl3) δ 7.79 (d, J = 7.7 Hz, 2H), 7.57 – 7.51 (m, 1H), 7.49 – 7.40 (m, 2H), 3.93 – 3.85 (m, 5H), 3.72 (s, 3H), 2.80 (s, 6H). 13

C NMR (100 MHz, CDCl3) δ 186.6, 169.5, 164.6, 155.8, 146.2, 140.0, 132.2, 129.0,

128.4, 126.9, 118.4, 52.6, 52.1, 43.8, 35.8. HRMS (EI) calcd for C18H19NO5S [M]+: 361.0978, found: 361.0983. Methyl 4-(dimethylamino)-2-(2-methoxy-2-oxoethyl)-5-(4-methoxybenzoyl) thiophene-3carboxylate (3ea) Yellow oil, 58.7 mg, 85% yield; 1H NMR (400 MHz, CDCl3) δ 7.81 (d, J = 8.8 Hz, 2H), 6.94 (d, J = 8.8 Hz, 2H), 3.91 – 3.86 (m, 8H), 3.73 (s, 3H), 2.78 (s, 6H). 13C NMR (100 MHz, CDCl3) δ 185.9, 169.6, 164.6, 163.1, 155.2, 145.3, 132.5, 131.5, 126.9, 118.7, 113.6, 55.6, 52.6, 52.1, 43.8, 35.8. ＋

HRMS (EI) calcd for C19H21NO6S [M] : 391.1084, found: 391.1086.

Methyl

5-(4-bromobenzoyl)-4-(dimethylamino)-2-(2-methoxy-2-oxoethyl)

thiophene-3-

carboxylate (3fa) Yellow oil, 41.3 mg, 47% yield; 1H NMR (400 MHz, CDCl3) δ 7.66 (d, J = 8.5 Hz, 2H), 7.59 (d, J = 8.5 Hz, 2H), 3.90 – 3.87 (m, 5H), 3.73 (s, 3H), 2.79 (s, 6H). 13C NMR (100 MHz, CDCl3) δ 185.4, 169.4, 164.5, 155.9, 146.5, 138.8, 131.6, 130.6, 127.0, 127.0, 118.1, 52.6, 52.2, 43.9, 35.8. HRMS (EI) calcd for C18H18BrNO5S [M]＋: 439.0084, found: 439.0082.

Dimethyl 3-(dimethylamino)-5-(2-methoxy-2-oxoethyl) thiophene-2,4-dicarboxylate (3ga) Yellow oil, 54.8 mg, 87% yield; 1H NMR (400 MHz, CDCl3) δ 3.89 – 3.84 (m, 5H), 3.81 (s, 3H), 3.73 (s, 3H), 2.93 (s, 6H).

13

C NMR (100 MHz, CDCl3) δ 169.6, 164.6, 161.4, 156.5, 144.6, 127.7,



Page 10 of 17

＋

111.1, 52.6, 52.1, 51.8, 43.8, 35.6. HRMS (EI) calcd for C13H17NO6S [M] : 315.0771, found: 315.0775. 2-Ethyl 4-methyl 3-(dimethylamino)-5-(2-methoxy-2-oxoethyl) thiophene-2,4-dicarboxylate (3ha) Yellow oil, 55.9 mg, 85% yield; 1H NMR (400 MHz, CDCl3) δ 4.27 (q, J = 7.1 Hz, 2H), 3.90 – 3.81 (m, 5H), 3.72 (s, 3H), 2.92 (s, 6H), 1.34 (t, J = 7.1 Hz, 3H). 13C NMR (101 MHz, CDCl3) δ 169.7, 164.6, 161.0, 156.3, 144.4, 127.8, 112.0, 60.7, 52.6, 52.1, 43.8, 35.6, 14.5. HRMS (EI) calcd for

C14H19NO6S [M]＋: 329.0928, found: 329.0932.

2-Tert-butyl

4-methyl

3-(dimethylamino)-5-(2-methoxy-2-oxoethyl)thiophene-2,4-

dicarboxylate（（3ia））

Yellow oil, 55.7 mg, 78% yield; 1H NMR (400 MHz, CDCl3) δ 3.86 – 3.84 (m, 5H), 3.72 (s, 3H), 2.91 (s, 6H), 1.54 (s, 9H). 13C NMR (100 MHz, CDCl3) δ 169.8, 164.6, 160.4, 155.5, 143.6, 127.9, ＋

114.3, 81.2, 52.6, 52.0, 43.7, 35.6, 28.5. HRMS (EI) calcd for C16H23NO6S [M] : 357.1241, found:

357.1243. 2-Benzyl

4-methyl

3-(dimethylamino)-5-(2-methoxy-2-oxoethyl)

thiophene-2,4-

dicarboxylate (3ja) Yellow oil, 57.9 mg, 74% yield; 1H NMR (400 MHz, CDCl3) δ 7.43 – 7.31 (m, 5H), 5.27 (s, 2H), 3.93 – 3.82 (m, 5H), 3.72 (s, 3H), 2.93 (s, 6H). 13C NMR (100 MHz, CDCl3) δ 169.6, 164.5, 160.6, 156.6, 144.8, 136.3, 128.7, 128.2, 128.0, 127.6, 110.8, 66.2, 52.6, 52.1, 43.8, 35.6. HRMS (EI) calcd for

C19H21NO6S [M]＋: 391.1084, found: 391.1086.


Page 11 of 17 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


Methyl 5-acetyl-2-(2-methoxy-2-oxoethyl)-4-morpholinothiophene-3-carboxylate (3ka) Yellow solid, 146-148 °C; 55.2 mg, 81% yield; 1H NMR (400 MHz, CDCl3) δ 3.91 (s, 2H), 3.89 (s, 3H), 3.83 (t, J = 4.7 Hz, 4H), 3.74 (s, 3H), 3.18 (t, J = 4.6 Hz, 4H), 2.59 (s, 3H).

13

C NMR

(100 MHz, CDCl3) δ 189.2, 169.5, 164.7, 152.8, 144.7, 129.6, 129.5, 67.4, 52.7, 52.3, 51.5, 35.5, 29.9. HRMS (EI) calcd for C15H19NO6S [M]＋: 341.0928, found: 341.0930.

Dimethyl 5-(2-methoxy-2-oxoethyl)-3-morpholinothiophene-2,4-dicarboxylate (3la) Yellow solid, m.p: 150-152 °C; 64.9 mg, 91% yield; 1H NMR (400 MHz, CDCl3) δ 3.89 (s, 2H), 3.87 (s, 3H), 3.83 (s, 3H), 3.82 – 3.78 (m, 4H), 3.73 (s, 3H), 3.27 – 3.17 (m, 4H).13C NMR (100 MHz, CDCl3) δ 169.6, 164.5, 161.3, 154.8, 144.3, 128.6, 115.4, 67.6, 52.7, 52.2, 52.0, 51.6, 35.4. HRMS (EI) calcd for C15H19NO7S [M]＋: 357.0877, found: 357.0883.

Dimethyl 3-(diethylamino)-5-(2-methoxy-2-oxoethyl) thiophene-2,4-dicarboxylate (3ma) Yellow oil, 56.3 mg, 82% yield; 1H NMR (400 MHz, CDCl3,) δ 3.89 (s, 2H), 3.84 (s, 3H), 3.81 (s, 3H), 3.73 (s, 3H), 3.23 (q, J = 7.1 Hz, 4H), 1.06 (t, J = 7.1 Hz, 6H). 13C NMR (100 MHz, CDCl3) δ 169.7, 164.6, 161.2, 155.4, 144.3, 129.7, 115.0, 52.6, 51.9, 51.7, 47.1, 35.6, 13.8. HRMS (EI) calcd for C15H21NO6S [M]＋: 343.1084, found: 343.1091.

Dimethyl 5-(2-methoxy-2-oxoethyl)-3-(methyl(phenyl)amino) thiophene-2,4-dicarboxylate (3na) Yellow solid, m.p: 75-77 °C; 64.1 mg, 85% yield; 1H NMR (400 MHz, CDCl3) δ 7.15 (dd, J = 7.3 Hz, 2H), 6.73 (d, J = 7.3 Hz, 1H), 6.59 – 6.53 (m, 2H), 4.08 (s, 2H), 3.79 (s, 3H), 3.75 (s, 3H), 3.45 (s, 3H), 3.28 (s, 3H).

13

C NMR (100 MHz, CDCl3) δ 169.7, 163.2, 160.7, 150.2, 148.4,



Page 12 of 17

146.4, 129.9, 129.0, 124.3, 118.1, 113.0, 52.7, 52.3, 51.9, 39.7, 35.4. HRMS (EI) calcd for C18H19NO6S [M]＋: 377.0928, found: 377.0932.

Methyl 5-(4-bromobenzoyl)-4-(dimethylamino)-2-(2-methoxy-2-oxoethyl) thiophene-3carboxylate （3oa）） Yellow oil, m.p: 75-77 °C; 53.2 mg, 57% yield; 1H NMR (400 MHz, CDCl3) δ 7.67 (d, J = 8.5 Hz, 2H), 7.58 (d, J = 8.5 Hz, 2H), 3.89 (s, 2H), 3.87 (s, 3H), 3.73 (s, 3H), 3.13 (q, J = 7.1 Hz, 4H), 1.06 (t, J = 7.1 Hz, 6H). 13C NMR (100 MHz, CDCl3) δ 185.4, 169.6, 164.7, 154.9, 145.5, 138.8, 131.6, 130.6, 128.7, 126.9, 120.6, 52.7, 52.1, 47.2, 35.6, 13.4. HRMS (EI) calcd for C20H22BrNO5S [M]＋: 467.0397, found: 467.0401.

Methyl 4-(dimethylamino)-5-(dimethylcarbamoyl)-2-(2-methoxy-2-oxoethyl) thiophene-3carboxylate (3pa) Yellow oil, 51.2 mg, 78% yield; 1H NMR (400 MHz, CDCl3) δ 3.90 (s, 2H), 3.88 (s, 3H), 3.72 (s, 3H), 3.06 (s, 6H), 2.79 (s, 6H). 13C NMR (101 MHz, CDCl3) δ 170.0, 165.1, 164.4, 149.9, 140.9, 126.6, ＋

117.6, 52.5, 52.0, 43.3, 35.5. HRMS (EI) calcd for C14H20N2O5S [M] : 328.1087, found: 328.1092.

4-Ethyl 2-methyl 3-(dimethylamino)-5-(2-ethoxy-2-oxoethyl) thiophene-2,4-dicarboxylate (3gb) Yellow oil, 57.6 mg, 84% yield; 1H NMR (400 MHz, CDCl3) δ 4.32 (q, J = 7.2 Hz, 2H), 4.18 (q, J = 7.1 Hz, 2H), 3.87 (s, 2H), 3.81 (s, 3H), 2.93 (s, 6H), 1.37 (t, J = 7.2 Hz, 3H), 1.27 (t, J = 7.2 Hz, 3H).

13

C NMR (100 MHz, CDCl3) δ 169.1, 164.2, 161.4, 156.5, 144.4, 128.2, 111.2, 61.6,


Page 13 of 17 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


＋

61.3, 51.7, 43.8, 35.8, 14.3, 14.2. HRMS (EI) calcd for C15H21NO6S [M] : 343.1084, found: 343.1091. ASSOCIATED CONTENT Supporting Information The Supporting Information is available free of charge on the ACS Publications website http://pubs.acs.org. Crystallographic data for compound 3la (CIF) Copies of 1H and 13C NMR spectra data for all compounds (PDF) AUTHOR INFORMATION Corresponding Author *E-Mail: [email protected]. *E-Mail: [email protected]. Notes The authors declare no competing financial interest. ACKNOWLEDGMENT This work is supported by the National Natural Science Foundation of China (No. 21572053) and Natural Science Foundation of Shanghai (No. 17ZR1407600). REFERENCES [1] (a) Morwick, T.; Berry, A.; Brickwood, J.; Cardozo, M.; Catron, K.; Deturi, M.; Emeigh, J.; Homon, C.; Hrapchak, M.; Jacober, S. J. Med. Chem. 2006, 49, 2898. (b) Haight, A. R.; Bailey, A. E.; Baker, W. S.; Cain, M. H.; Copp, R. R.; DeMattei, J. A.; Ford, K. L.; Henry, R. F.; Hsu, M. C.; Keyes, R. F. Org. Process. Res. Dev. 2004, 8, 897. (c) Redman, A. M.; Johnson, J. S.; Dally, R.;



Swartz, S.; Wild, H.; Paulsen, H.; Caringal, Y.; Gunn, D.; Renick, J.; Osterhout, M. Bioorg. Med. Chem. Lett. 2001, 11, 9. (d) Schulz, V.; Fischer, W.; Hanselle, U.; Huhmann, W.; Zietsch, V. Eur. J. Clin. Pharmacol. 1986, 31, 405. [2] (a) He, B.; Wenger, O. S. J. Am. Chem. Soc. 2011, 133, 17027. (b) Collado, D.; Casado, J.; Rodriguez Gonzalez, S.; Lopez Navarrete, J. T.; Suau, R.; Perez-Inestrosa, E.; Pappenfus, T. M.; Raposo, M. M. Chem. - Eur. J. 2011, 17, 498. (c) Douglas, J. J.; Albright, H.; Sevrin, M. J.; Cole, K. P.; Stephenson, C. R. J. Angew. Chem., Int. Ed. 2015, 54, 14898. [3] For selected reviews of thiophene synthesis (a) Mishra, R.; Tomar, I.; Kumar, S.; Jha, K. K. Der. Pharma. Chemica. 2011, 3, 38. (b) Mancuso, R.; Gabriele, B. Molecules. 2014, 19, 15687. (c) Nogi, K.; Yorimitsu, H. Chem. Commun. 2017, 53, 4055. [4] Functionalization of thiophene, see: (a) Okazawa, T.; Satoh, T.; Masahiro Miura, A.; Nomura, M. J. Am. Chem. Soc. 2002, 124, 5286. (b) Tsai, C. H.; Chirdon, D. N.; Maurer, A. B.; Bernhard, S.; Noonan, K. J. Org. Lett. 2013, 15, 5230. (c) Junker, A.; Yamaguchi, J.; Itami, K.; Wunsch, B. J. Org. Chem. 2013, 78, 5579. (d) Denoyelle, S.; Tambutet, G.; Masurier, N.; Maillard, L. T.; Martinez, J.; Lisowski, V. Eur. J. Org. Chem. 2015, 32, 7146. [5] For selected recent examples of the cycloaddition of sulfur-containing compounds, see: (a) Liang, F.; Li, D.; Zhang, L.; Gao, J.; Liu, Q. Org. Lett. 2007, 9, 4845. (b) Henssler, J. T.; Matzger, A. J. Org. Lett. 2009, 11, 3144. (c) Zhang, Y.; Bian, M.; Yao, W.; Gu, J.; Ma, C. Chem. Commun. 2009, 40, 4729. (d) Zhou, H.; Xie, Y.; Ren, L.; Su, R. Org. Lett. 2010, 12, 356. (e) Nandi, G. C.; Samai, S.; Singh, M. S. J. Org. Chem. 2011, 76, 8009. (f) Fang, Z.; Yuan, H.; Liu, Y.; Tong, Z.; Li, H.; Yang, J.; Barry, B. D.; Liu, J.; Liao, P.; Zhang, J.; Liu, Q.; Bi, X. Chem. Commun. 2012, 48, 8802. (g) Gabriele, B.; Mancuso, R.; Salerno, G.; Larock, R. C. J. Org. Chem. 2012, 77, 7640. (h) Ramulu, B. J.; Koley, S.; Singh, M. S. Org. Biomol. Chem. 2016, 14, 434.


Page 14 of 17

Page 15 of 17 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


[6] (a) Kathiravan, M. K.; Shishoo, C. J.; Chitre, T. S.; Mahadik, K. R.; Jain, K. S. Synth. Commun. 2007, 37, 4273. (b) You, W.; Yan, X.; Liao, Q.; Xi, C. Org. Lett. 2010, 12, 3930. (c) Huang, X.-G.; Liu, J.; Ren, J.; Wang, T.; Chen, W.; Zeng, B.-B. Tetrahedron. 2011, 67, 6202. (d) Reddy, C. R.; Valleti, R. R.; Reddy, M. D. J. Org. Chem. 2013, 78, 6495. (e) Liao, Q.; You, W.; Lou, Z.-B.; Wen, L.-R.; Xi, C. Tetrahedron. Lett. 2013, 54, 1475. (f) Liu, W.; Chen, C.; Liu, H. Adv. Synth. Catal. 2015, 357, 4050. (g) Rao, M. L. N.; Islam, S. S.; Dasgupta, P. RSC. Adv. 2015, 5, 78090. [7] For selected reviews of thioamide: (a) Kumagai N.; Shibasaki, M. Isr. J. Chem. 2012, 52, 604. (b) Guo, W. S.; Wen, L. R.; Li, M. Org. Biomol. Chem. 2015, 13, 1942. [8] (a) Ransborg, L. K.; Albrecht, L.; Weise, C. F.; Bak, J. R.; Joergensen, K. A. Org. Lett. 2012, 14, 724. (b) Jalani, H. B.; Pandya, A. N.; Pandya, D. H.; Sharma, J. A.; Sudarsanam, V.; Vasu, K. K. Tetrahedron. Lett. 2012, 53, 6927. (c) Wen, L. R.; He, T.; Lan, M. C.; Li, M. J. Org. Chem. 2013, 78, 10617. (d) Ge, L. S.; Wang, Z. L.; An, X. L.; Luo, X.; Deng, W. P. Org. Biomol. Chem. 2014, 12, 8473. (e) Zhang, X.; Wu, M.; Zhang, J.; Cao, S. Org. Biomol. Chem. 2017, 15, 2436. [9] (a) Wang, Z. L.; Li, H. L.; Ge, L. S.; An, X. L.; Zhang, Z. G.; Luo, X.; Fossey, J. S.; Deng, W. P. J. Org. Chem. 2014, 79, 1156. (b) Luo, X.; Ge, L. S.; An, X. L.; Jin, J. H.; Wang, Y.; Sun, P. P.; Deng, W. P. J. Org. Chem. 2015, 80, 4611. [10] (a) Zhang, L.; Li, X.; Liu, Y.; Zhang, D. Chem. Commun. 2015, 51, 6633. (b) He, Y.; Zhang, X.; Fan, X. Chem. Commun. 2015, 51, 16263. (c) Hosseyni, S.; Su, Y.; Shi, X. Org. Lett. 2015, 17, 6010. (d) Zi, W.; Toste, F. D. Angew. Chem., Int. Ed. 2015, 54, 14447. (e) Kondoh, A.; Ishikawa, S.; Aoki, T.; Terada, M. Chem. Commun. 2016, 52, 12513. (f) Zhou, Q. F.; Zhang, K.; Cai, L.; Kwon, O. Org. Lett. 2016, 18, 2954. (g) Lin, W.; Cheng, J.; Ma, S. Adv. Synth. Catal. 2016, 358, 1989. (h) Zhou, X.; Huang, C.; Zeng, Y.; Xiong, J.; Xiao, Y.; Zhang, J. Chem. Commun. 2017, 53,



1084. (i) Naidu, V. R.; Posevins, D.; Volla, C. M.; Backvall, J. E. Angew. Chem., Int. Ed. 2017, 56, 1590. [11] (a) Liao, J. Y.; Shao, P. L.; Zhao, Y. J. Am. Chem. Soc. 2015, 137, 628. (b) Wang, D.; Wang, G.-P.; Sun, Y.-L.; Zhu, S.-F.; Wei, Y.; Zhou, Q.-L.; Shi, M. Chem. Sci. 2015, 6, 7319. (c) Wang, Y.; Zhang, P.; Qian, D.; Zhang, J. Angew. Chem., Int. Ed. 2015, 54, 14849. (d) Yao, W.; Dou, X.; Lu, Y. J. Am. Chem. Soc. 2015, 137, 54. (e) Ni, C.; Wang, M.; Tong, X. Org. Lett. 2016, 18, 2240. (f) Cai, L.; Zhang, K.; Kwon, O. J. Am. Chem. Soc. 2016, 138, 3298. (g) Ni, H.; Yao, W.; Waheed, A.; Ullah, N.; Lu, Y. Org. Lett. 2016, 18, 2138. (h) Ni, C.; Zhang, Y.; Hou, Y.; Tong, X. Chem. Commun. 2017, 53, 2567. (i) Zhou, W.; Ni, C.; Chen, J.; Wang, D.; Tong, X. Org. Lett. 2017, 19, 1890. [12] (a) Li, H. L.; Wang, Y.; Sun, P. P.; Luo, X.; Shen, Z.; Deng, W. P. Chem. - Eur. J. 2016, 22, 9348. (b) Wang, Y.; Jiang, C.-M.; Li, H. L.; He, F. S.; Luo, X.; Deng, W.-P. J. Org. Chem. 2016, 81, 8653. [13] (a) Xie, J.; Jiang, H.; Cheng, Y.; Zhu, C. Chem. Commun. 2012, 48, 979. (b) Boominathan, S. S.; Hu, W. P.; Senadi, G. C.; Vandavasi, J. K.; Wang, J. J. Chem. Commun. 2014, 50, 6726. (c) Gao, W. C.; Hu, F.; Huo, Y. M.; Chang, H. H.; Li, X.; Wei, W. L. Org. Lett. 2015, 17, 3914. (d) Tang, S.; Liu, K.; Long, Y.; Gao, X.; Gao, M.; Lei, A. Org. Lett. 2015, 17, 2404. (e) Zhou, Z.; Cheng, J.; Yu, J. T. Org. Biomol. Chem. 2015, 13, 9751. (f) Gao, W. C.; Hu, F.; Tian, J.; Li, X.; Wei, W. L.; Chang, H. H. Chem. Commun. 2016, 52, 13097. (g) Chen, C.; Liu, W.; Zhou, P.; Liu, H. RSC Adv. 2017, 7, 20394. (h) Peng, Y.; Liu, J.; Qi, C.; Yuan, G.; Li, J.; Jiang, H. Chem. Commun. 2017, 53, 2665. (i) Wang, D.; Zhang, K.; Jia, L.; Zhang, D.; Zhang, Y.; Cheng, Y.; Lin, C.; Wang, B. Org. Biomol. Chem. 2017, 15, 3427. [14] (a) Parvatkar, P. T.; Parameswaran, P. S.; Tilve, S. G. Chem. - Eur. J. 2012, 18, 5460. (b)


Page 16 of 17

Page 17 of 17 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


Shibahara, F.; Kitagawa, A.; Yamaguchi, E.; Murai, T. Org. Lett. 2006, 8, 5621. (c) Downer-Riley, N. K.; Jackson, Y. A. Tetrahedron. 2007, 63, 10276. (d) Wen, L.-R.; Men, L.-B.; He, T.; Ji, G.-J.; Li, M. Chem. - Eur. J. 2014, 20, 5028. [15] (a) Liu, Q.; Rovis, T. Org. Lett. 2009, 11, 2856. (b) Zhang, Y.-L.; Xiao, J.-M.; Feng, J.-L.; Yang, K.-W.; Feng, L.; Zhou, L.-S.; Crowder, M. W. Bioorg. Med. Chem. Lett. 2013, 23, 1676. (c) Bhunia, S.; Ghosh, S.; Dey D.; Bisai, A. Org. Lett. 2013, 15, 2426. (d) Kim, M.-H.; Choi, S.-H.; Lee, Y.-J.; Lee, J.; Nahm, K.; Jeong, B.-S.; Park, H.-G.; Jew, S.-S. Chem. Commun. 2009, 40, 782.


Synthesis of Polysubstituted 3-Aminothiophenes from Thioamides and

Recommend Documents