## 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‐acety
The preparation of tritium labeled methadone and its metabolites
✍ Scribed by Herbert H. Seltzman; Steven D. Wyrick; Colin G. Pitt
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- French
- Weight
- 430 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
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 specific introduction of tritium without scrambling. (+)‐Methadone‐1‐^3^H (25 Ci/mmole) was obtained by oxidation of (‐)‐methadol‐1,2‐^3^H~2~ followed by sodium hydroxide exchange of the 2‐^3^H.
📜 SIMILAR VOLUMES
## Abstract A method for preparing tritium‐labelled ryanodine is described. The alkaloid was first brominated, and the bromoryanodines were separated from the reaction mixture by thin layer chromatography; NMR analysis at this stage showed substitution of pyrrole protons by bromine. Bromoryanodine
Dimethylnitrosamine, nitrosomorpholine, nitrosopyrrolidine, nitrosopiperidine, nitrosoazetidine, hexamethylenenitrosamine, nitrosornethylcyclohexylamine, nitrosomethylaniline and dinitrosopiperazine have been prepared labeled with tritium by nifrosation of the corresponding amines which had been lab
Aflatoxins BI and G1 were labeled with tritium by reaction with tritiated water in the presence of a catalyst. Although considerable decomposition occurred, it was possible to purify the products by thin layer chromatography and crystallization following addition of unlabeled compound. The products
## Abstract The synthesis of d, l, ‐12‐bromocamptothecin (**2d**) from camptothecin (**1**) is described. Reduction of the bromo derivative **2d** with tritium gas in the presence of palladium on carbon afforded d, l‐camptothecin 12‐^3^H having a specific activity of 29 Ci/mmol. A simpler labelling
## Abstract A procedure is described for incorporating tritium into the 3‐CH~2~ side chain of synthanecine A, and preparing the carbamate, 2,3‐bis‐N‐ethylcarbamoyloxymethyl‐l‐methyl‐3‐pyrroline, a hepatotoxic pyrrolizidine alkaloid analogue. The pyrrolizidine amino alcohol, retronecine, can be trit