𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of 3H and 14C labelled SCH 48461

✍ Scribed by D. Hesk; C. Bowlen; S. Hendershot; D. Koharski; P. McNamara; D. Rettig; S. Saluja


Publisher
John Wiley and Sons
Year
1996
Tongue
French
Weight
404 KB
Volume
38
Category
Article
ISSN
0022-2135

No coin nor oath required. For personal study only.

✦ Synopsis


3H-Sch 47949, racemic 3H-Sch 48461, was prepared at a specific activity of 40 mCi/mmole by Pt catalysed exchange with tritiated water. 3H-Sch 48461 was prepared at a specific activity of 64.6 Ci/mmole by a Pd/C catalysed reduction of an olefinic intermediate. 14C-Sch 48461 was prepared in 8 steps from 14Cpotassium cyanide with an overall radiochemical yield of 18.5%.


πŸ“œ SIMILAR VOLUMES


Synthesis of 3H-SCH 51048 and 14C-SCH 56
✍ C. V. Magatti; D. Hesk; M. J. Lauzon; S. S. Saluja; X. Wang πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 French βš– 351 KB
Synthesis of 14C-labelled satigrel
✍ Shigeru Tanaka; Youji Yamagishi; Kazutomi Kusano; Tsutomu Yoshimura πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 French βš– 222 KB πŸ‘ 1 views

14C-Labelled satigrel, or 4-cyano-5-(4'-methoxy tring-U-14CI phenyl)-5-(4"methoxyphenyl)-4-pentenoic acid was synthesized for drug metabolism and pharmacokinetic studies using 4,4'-diniethoxy [ring-U-W ] benzophenone as the starting material. The radiochemical yield was 10.0%. The specific radioacti

Synthesis of 3H and 14C-SCH 27899 by fer
✍ D. Hesk; I. Gunnarsson; S. Hendershot; D. Koharski; P. McNamara; J. L. Schwartz; πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 French βš– 406 KB

\({ }^{3} \mathrm{H}\) and \({ }^{14} \mathrm{C}\)-Sch 27899 have been prepared by fermentation using the Micromonospora carbonacea organism. In the case of \({ }^{3} \mathrm{H}\)-Sch 27899 , the label was incorporated by a single addition of \(100 \mathrm{mCi}\) of \(70 \mathrm{Ci} / \mathrm{mmole}

Synthesis of 14C-labeled levamisole and
✍ V. J. Feil πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 French βš– 275 KB πŸ‘ 2 views

The syntheses of '%-ring labeled levamisole ([-)-2,3,5,6-tetrahydr0-6-phenyl[~'C-UL]imidazo(Z, 1b]thiole) from acetophenone-ring-UL-l'C in 5 steps plus resolution with a 7.5% overall yield, and %,-ring labeled tetramisole ([i]-2,3,5,6-tetrahydro-6-phenyif3 S ]imidaz0[2,?-bjthiazole) from benzene-'%,