Synthesis of 2,4′,5-trichloro [14C]biphenyl mercapturic acids
The synthesis of 3‐ and 4‐S‐(N‐acetyl)cysteinyl‐2,4′,5‐trichloro[14C]biphenyl is described. 4‐Chloro[14C]aniline was used as starting material. The products were obtained after an aryl coupling of the amine with 2,5‐dichloronitrobenzene, a reduction of the nitrogroup and finally coupling of the diaz...
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Veröffentlicht in: | Journal of labelled compounds & radiopharmaceuticals 1983-08, Vol.20 (8), p.961-966 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | The synthesis of 3‐ and 4‐S‐(N‐acetyl)cysteinyl‐2,4′,5‐trichloro[14C]biphenyl is described. 4‐Chloro[14C]aniline was used as starting material. The products were obtained after an aryl coupling of the amine with 2,5‐dichloronitrobenzene, a reduction of the nitrogroup and finally coupling of the diazotized trichlorobiphenyl amine with cuprous N‐acetylcysteine mercaptide. |
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ISSN: | 0362-4803 1099-1344 |
DOI: | 10.1002/jlcr.2580200806 |