Benzylamine → cis-8-Benzoyl-5-benzyl-2-oxa-5,8-diazabicyclo[4.3.0]nonane

HRID 374553

반응식

HRID 374553 반응식
[C:1]([N:9]1[CH2:13][C@@H:12]([O:14][CH2:15][CH2:16]OS(C2C=CC(C)=CC=2)(=O)=O)[C@H:11](Br)[CH2:10]1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:29]([NH2:36])[C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1>C1(C)C(C)=CC=CC=1>[C:1]([N:9]1[CH2:13][C@@H:12]2[C@@H:11]([N:36]([CH2:29][C:30]3[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=3)[CH2:16][CH2:15][O:14]2)[CH2:10]1)(=[O:8])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

참가 물질

4

실험 절차

124 g (0.265 mol) of trans-1-benzoyl-3-bromo-4-(2-tosyloxyethoxy)-pyrrolidine are heated under reflux overnight in 1.5 1 of xylene together with 86 g 0.8 mol) of benzylamine. The salts of the benzylamine are filtered off with suction and the filtrate is concentrated.

후처리

  1. filtrationThe salts of the benzylamine are filtered off with suction
  2. concentrationthe filtrate is concentrated

출처 및 근거

ORD 기록
ord-198d28caa75146abba072ad94f80ad82
출처 데이터셋
uspto-grants-1996_01
특허 번호
US05480879

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