## Abstract The synthesis and catalytic tritium reduction of 1,2‐dehydro analogs of (‐)‐methadol, (‐)‐α‐acetylmethadol, and (‐)‐α‐acetyl‐N‐normethadol afforded the labeled compounds with high specific activity (44‐60 Ci/ mmole). The use of the homogeneous catalyst (ϕ~3~P)~3~RhCl resulted in specifi
Preparation of methadone and some congeners labeled with tritium in the aromatic rings
✍ Scribed by J. A. Kepler; C. M. Sparacino; C. R. Howe; R. D. Austin
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- French
- Weight
- 416 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
[diphenyl‐2,2′‐^3^H~2~]Methadone with specific activity of 8‐30 Ci/mmol was prepared by reductive dehalogenation of 6‐dimethylamino‐4, 4‐bis(2‐chlorophenyl)‐3‐heptanone with carrier‐free tritium gas. The labeled congeners (−)‐α‐acetylmethadol, (−)‐α‐acetyl‐N‐normethadol, and (−)‐α‐acetyl‐N,N‐dinormethadol were prepared from (+)‐[diphenyl‐2,2′‐^3^H~2~]methadone.
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