1-((tert-Butoxycarbonyl)amino)cyclopropanecarboxylic acid → Ethyl 3-(1-{[(tert-butoxy)carbonyl]amino}cyclopropyl)-3-oxopropanoate
반응식
[C:1]([O:5][C:6]([NH:8][CH2:9][C:10](=[O:17])[CH2:11][C:12]([O:14][CH2:15][CH3:16])=[O:13])=[O:7])([CH3:4])([CH3:3])[CH3:2].C(NC1(C(O)=O)CC1)(O[C:21](C)(C)[CH3:22])=O>>[C:1]([O:5][C:6]([NH:8][C:9]1([C:10](=[O:17])[CH2:11][C:12]([O:14][CH2:15][CH3:16])=[O:13])[CH2:22][CH2:21]1)=[O:7])([CH3:3])([CH3:4])[CH3:2]참가 물질
3
실험 절차
A tautomeric mixture of ethyl 3-(1-((tert-butoxycarbonyl)amino)cyclopropyl)-3-oxopropanoate and (Z)-ethyl 3-(1-((tert-butoxycarbonyl)amino)cyclopropyl)-3-hydroxyacrylate (3.15 g, 11.61 mmol, 90% yield) as an off white solid was prepared according the procedures described for Intermediate 601, using 1-(Boc-amino)cyclopropanecarboxylic acid (Chem-Impex International, Inc., cat #04052) (2.59 g, 12.87 mmol) as the reagent. m/z (ESI, +ve) 294.2 (M+23)+.
후처리
- customwas prepared
출처 및 근거
- ORD 기록
- ord-334910615d7444ad96af360f66e96e68
- 출처 데이터셋
- uspto-grants-2016_07
- 특허 번호
- US09394297B2
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