## Abstract The syntheses of 4‐amino‐3,2′‐dimethyl‐biphenyl‐3‐methyl‐^14^C, a potent carcinogen and mutagen, and 4‐amino‐2′‐methylbiphenyl‐2′‐methyl‐^14^C, an analogue having weaker activity, are described. In both cases, label was introduced with Cu^14^ CN.
Synthesis of (2S : 3R)-4-Dimethylamino-l, 2-diphenyl-3-methyl-2-propionoxybutane-l-14C, d-Propoxyphene-l-14C
✍ Scribed by J. A. Kepler; G. F. Taylor
- Publisher
- John Wiley and Sons
- Year
- 1970
- Tongue
- French
- Weight
- 114 KB
- Volume
- 6
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
d-Propoxyphene, first synthesized by Pohland and Sullivan (la), is a commonly used analgesic. Metabolism studies (2) on racemic N-methyl-14C propoxyphene (3) established that the major metabolic product is the N-demethylated compound. Analytical and metabolic studies performed on d-propoxyphene in these laboratories required optically active radiolabeled drug in which the label would be metabolically secure. The availability of benzylchloride-7-14C suggested the preparation of d-propoxyphene labeled at C-1 .
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