## Abstract 3‐Benzylamino‐8, 9‐dimethoxy‐5, 6‐dihydro‐imidazo‐ [5,1‐a] isoquinoline hydrochloride was labelled with ^14^C in two different positions: In one case the ^14^C was built into the position 2 of the imidazole ring, in the other case into the position 3 of the isoquinoline ring. In the fir
Potential drugs labelled with 14C. II. Synthesis of 1-cyano-3-imino-8, 9-dimethoxy-3, 4,5,6- -tetrahydro-thiazolo[4, 3-a]isoquinoline hydrochloride
✍ Scribed by E. Koltai; G. Zólyomi; P. Komáromy; D. Bánfi; T. Szüts; K. Takács
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- French
- Weight
- 295 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
The synthesis of 1‐cyano‐3‐imino‐8,9‐dimethoxy‐ ‐3,4, 5,6‐tetrahydro‐thiazolo [4,3‐a]isoquinoline hydrochloride labelled with ^14^C in five different positions: in position 3 (1a), in the cyano group at position 1 (1b), in position 5 (1c), in position 10b (1d) and in the methoxy groups at position 8 and 9 (1e) was carried out.
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## Abstract ^14^C‐Labelled (S)‐(+)‐6‐(2‐chlorophenyl)‐3‐cyclopropanecarbonyl‐8,11‐dimethyl‐2,3,4,5‐ tetrahydro‐8H‐pyrido[4′,3′:4,5]thieno[3,2‐f][1,2,4]triazolo[4,3‐a][1,4] diazepine (^14^C‐E6123), a platelet activating factor receptor antagonist for studying the pharmacokinetic profile of E6123, wa
## Abstract 2‐Propyl‐8‐oxo‐1‐[(2′‐(1H‐tetrazole‐5‐yl) biphenyl‐4‐yl)methyl]‐4, 5, 6, 7‐tetrahydrocyclohept imidazole (KT3‐671), which has been found to be a potent and selective angiotesin II receptor antagonist, was synthesized in ^14^C‐labelled form by using potassium[^14^C]‐cyanide. [^14^C](KT3‐