반응식
[C:1]([O:5][C:6]([CH2:8][N:9]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH:11]=[C:10]1[C:18](O)=[O:19])=[O:7])([CH3:4])([CH3:3])[CH3:2].C(N1CCOCC1)C.Cl.[CH:30]([N:33]1[CH2:38][CH2:37][CH:36]([NH2:39])[CH2:35][CH2:34]1)([CH3:32])[CH3:31]>ClCCl>[CH:30]([N:33]1[CH2:38][CH2:37][CH:36]([NH:39][C:18]([C:10]2[N:9]([CH2:8][C:6]([O:5][C:1]([CH3:4])([CH3:3])[CH3:2])=[O:7])[C:17]3[C:12]([CH:11]=2)=[CH:13][CH:14]=[CH:15][CH:16]=3)=[O:19])[CH2:35][CH2:34]1)([CH3:32])[CH3:31]참가 물질
실험 절차
To a solution of 0.5 g 1-tert.-butoxycarbonylmethyl-1H-indole-2-carboxylic acid and 0.91 ml N-ethylmorpholine in 3 ml dichloromethane 0.6 g O-[(ethoxycarbonyl)cyanomethylenamino]-N,N,N′,N′-tetramethyluronium tetrafluoroborate were added and the mixture was stirred for 30 min at room temperature. 0.39 g 1-isopropyl-piperidin-4-ylamine hydrochloride were added to the mixture and the reaction mixture was further stirred for 1 hour. After removal of the solvent under reduced pressure the residue was partitioned between 15 ml water and 15 ml dichloromethane. The organic layer was washed with additional water and then dried over sodium sulphate. After filtration the solvent was removed under reduced pressure and a white solid was obtained. The residue was directly subjected to the subsequent reaction without further purification.
후처리
- stirringthe reaction mixture was further stirred for 1 hour
- customAfter removal of the solvent under reduced pressure the residue
- customwas partitioned between 15 ml water and 15 ml dichloromethane
- washThe organic layer was washed with additional water
- dry with materialdried over sodium sulphate
- filtrationAfter filtration the solvent
- customwas removed under reduced pressure
- customa white solid was obtained
- customThe residue was directly subjected to the subsequent reaction without further purification
출처 및 근거
- ORD 기록
- ord-37a5fa146fd443cfb9fd198d77a370cf
- 출처 데이터셋
- uspto-grants-2005_06
- 특허 번호
- US06906084B2
연결된 노트
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