## Abstract Two benzodiazepine CCK antagonists __N__‐(2,3‐dihydro‐1‐[^14^C]methyl‐2‐oxo‐5‐phenyl‐1H 1,4‐benzodiazepin‐3‐yl)‐benzamide **2** and __N__‐(2,3‐dihydro‐1‐[^14^C]methyl‐2‐oxo‐5‐phenyl‐1H‐1,4‐benzodiazepin‐3‐yl)‐[^14^C]methyl‐benzamide **3** were synthesized in high yields through the reac
Labelling of a mucolytic agent with carbon-14 synthesis of N-[2-(N′-cyclohexyl-N′-methyl-N′-methylene)-4,6-dibromo-phenyl]-3-methoxy-4-acetoxy-benzamide, hydrochloride
✍ Scribed by Victor Rimbau
- Publisher
- John Wiley and Sons
- Year
- 1978
- Tongue
- French
- Weight
- 134 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract A new potent neuroleptic agent YM‐09151‐2, N‐[(2RS, 3RS)‐1‐benzyl‐2‐methyl‐3‐pyrrolidinyl]‐5‐chloro‐2‐methoxy‐4‐ (methylamino) benzamide (**10c**), was labeled with carbon‐14 and deuterium for biochemical studies such as metabolism and 14 pharmacokinetics. The synthesis of [carbonyl‐^14
## Abstract __N__‐(1‐methyl‐2‐oxo‐5‐phenyl‐2,3‐dihydro‐1H‐benzo[e][1,4]diazepin‐3‐yl)‐benzamide‐[carboxyl‐^14^C] has been synthesized from benzonitrile‐[cyano‐^14^C]. Copyright © 2005 John Wiley & Sons, Ltd.
Syn thes is of 14C -labe 1 led 4 -chloro -3 -s u l f amoyl -N -(3aa, 4a, 5 , 6 7a,7aa-hexahydro-4,7-methano-isoindolin-Z-yl)-benzamide.