Benzhydrylamine → N-(Diphenylmethyl)-3-oxo-4-azaandrost-5-ene-17beta-carboxamide

HRID 1463938노트

반응식

HRID 1463938 반응식
[O:1]=[C:2]1[CH2:19][CH2:18][C@@:17]2([CH3:20])[C:4](=[CH:5][CH2:6][C@@H:7]3[C@@H:16]2[CH2:15][CH2:14][C@@:12]2([CH3:13])[C@H:8]3[CH2:9][CH2:10][C@@H:11]2[C:21](O)=[O:22])[NH:3]1.[C:24]1([CH:30]([NH2:37])[C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=2)[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1>>[C:24]1([CH:30]([C:31]2[CH:32]=[CH:33][CH:34]=[CH:35][CH:36]=2)[NH:37][C:21]([C@H:11]2[CH2:10][CH2:9][C@H:8]3[C@H:7]4[C@H:16]([CH2:15][CH2:14][C@:12]23[CH3:13])[C@:17]2([CH3:20])[C:4]([NH:3][C:2](=[O:1])[CH2:19][CH2:18]2)=[CH:5][CH2:6]4)=[O:22])[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1

참가 물질

3

반응물 2

HCID 7036BenzhydrylamineHCID 4754473-Oxo-4-aza-5-androstene-17beta-carboxylic acid

생성물 1

HCID 67750903N-(Diphenylmethyl)-3-oxo-4-azaandrost-5-ene-17beta-carboxamide수율 59%

실험 절차

The title compound was prepared in a yield of 59% in a similar manner to that described in Example 1 by reacting 3-oxo-4-azaandrost-5-ene-17β-carboxylic acid and diphenylmethylamine.

출처 및 근거

ORD 기록
ord-1ce103aac82f477eadd887a58006ae0c
출처 데이터셋
uspto-grants-1994_04
특허 번호
US05302621

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