Synthesis of Reserpine Analogs1, 2

Synthesis of Reserpine Analogs1,2. FRED A. TURNER, and JAMES E. GEARIEN. J. Org. Chem. , 1959, 24 (12), pp 1952–1955. DOI: 10.1021/jo01094a031...
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1952

VOL.

TURNER AND GEARIEN [ C O X T R l I i L T I O X F R O N THE

DEPARTMENT OF CHEMISTRY.

24

C O L L E G E O F P H A R M A C Y , U N I V E R S I T Y OF ILLINOIS]

Synthesis of Reserpine Analogs'j2 FRED A. TURNER

AND

JAMES E. GEARIES

Received June $9, 1959 Esters of methyl 3-hydroxy-5-piperidinomethylbenzoate and of methyl 3-hydroxy-5-diethylaniinomethylbenzoatewere prepared and subjected to pharmacological testing. These compounds, resembling in structure a portion of the reserpine molecule, failed to show appreciable pharmacological activity. Esters of 3-piperidinomethylphenol, 3-diethylaminomethplphenol, 3-piperidinomethylbenzoic acid, and 3-diethylaminobenzoic acid were also prepared and were without pharmacological activity. All compounds were obtained as their hydrochlorides.

Esters of methyl 3-hydroxy-5-piperidinomethylbenzoate and of methyl 3-hydroxy-&diethylaminomethylbenzoate (I) may be regarded as analogs of a portion of the reserpine molecule (11).The above CH2-R .HCl

CHAOC

I

OR 1

methylbenzoate, the benzoic acid ester (Ib) and the 3,4,5-trimethoxybenzoic acid ester (Id) of methyl 3-hydroxy-5-diethylaminomethylbenzoate were prepared as their hydrochlorides. In the hope of observing the effects of further modification of molecular structure upon pharmacological activity, similar esters of 3-piperidinomethylphenol (IIIa and IIIc) and 3-diethylaminomethylphenol (IIIb and IIId), as well as the methyl esters of 3-piperidinomethylbenzoic acid (IVa) and 3-diethylaminomethylbenzoic acid (IVb) , mere also synthesized as their hydrochlorides.

OCHa

OCH

Ia. R Ib. R IC. R Id. R

= = = =

\

. HC1 OCHi

I1 piperidino, R1 = acetyl diethylamino, Rl = benzoyl piperidino, R1 = 3,4,5-trimethoxybenxoyl diethylamino, R1 = 3,4,5-trimethoxybenzoyl

compounds possess ring E of the reserpine molecule as an :aromatic ring, a portion of ring D, and all or a portion of ring C. The aromatic ring is substituted similarly to ring E of the reserpine molecule, except that the C-17 methoxyl group has been omitted. The presence of this group mas deemed unnecessary t o pharmacological activity since 17-desmethoxyde