## Abstract The title compound 9 was prepared by the route outlined in Scheme I. [^14^C]Thiourea (1) was condensed with ethyl 4‐bromo‐3‐oxo‐2‐methoxyiminoacetate (2), providing ethyl 2‐(2‐amino‐4‐[2‐^14^C]thiazolyl)‐2‐methoxyiminoacetate (3), as the pure Z‐isomer. Saponification gave the amino acid
Synthesis of N-[4-(2-dimethylaminoethoxy) benzyl-α-14C]-3,4,5-trimethoxybenzamide hydrochloride and N-[4-(2- methylaminoethoxy)benzyl-α-14C]-3, 4-diethoxybenzamide hydrochloride
✍ Scribed by R. L. Wineholt; J. D. Johnson; P. J. Heck; H. H. Kaegi
- Publisher
- John Wiley and Sons
- Year
- 1970
- Tongue
- French
- Weight
- 394 KB
- Volume
- 6
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
The anti-emetic compounds N-[4-(2-dimethylaminoethoxy
j benzyla-f4C]-3,4,5-trimethoxybenzamide hydrochloride (10) and N44-(2-methylaminoethoxy)benzyl-a-f~C]-3,4-diethoxybenzamide hydrochloride ( 1 1 j were prepared. The synthesis of 10 in four steps provided the purijied material in 29 % yield from carbon dioxide. The same series of reactions was used to prepare N-[4-(2-benzylmethylaminoethoxy) benzyl-a-14CC]-3,4-diethoxybenzamide (9), which after an additional debenzylation step furnished 1 1 in 56 % yield based on carbon dioxide.
📜 SIMILAR VOLUMES
## Abstract ^14^C‐Labelled __N__‐(2‐chloro‐3,4‐dimethoxybenzylideneamino)guanidinium acetate has been synthesized as a part of a four‐step procedure which involved decarboxylation of 2‐chloro‐3,4‐dimethoxybenzoic acid by Pb(OAc)~4~ to give 2‐chloro‐3,4‐dimethoxy‐1‐iodobenzene, followed by a selecti
## Synthesis of the title compound ( 5 ) . an histamine H2 -receptor antagonist, is described. Treatment of 3-(3-[2.6-C1-piperidinomethylphenoxv)propylamine(l)l with 3-amino-4-methoxy-l,2,5-thiadiazole-1-oxide2 produced 3-amino-4-13-0-[ 2,6-"C]piperidinomethylphenoxy)propylamino~-1,2,5-thiadiazole
## Abstract The title compound (1) was synthesized by a 7‐step sequence. 4‐Amino‐2‐hydroxy‐[carbonyl‐^14^C]benzoic acid (1) was selectively methylated to provide the ether ester 2, which was smoothly chlorinated in acetic acid to give 3. The ester was hydrolyzed with aqueous potassium hydroxide to