반응식
[CH2:1]([O:8][C:9]1[CH:27]=[CH:26][C:25]([Br:28])=[CH:24][C:10]=1[CH2:11][N:12]([C:15]1[CH:20]=[CH:19][C:18]([C:21]([OH:23])=O)=[CH:17][N:16]=1)[CH2:13][CH3:14])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:29]([S:32]([NH2:35])(=[O:34])=[O:33])[CH2:30][CH3:31].CN(C1N=CC=CN=1)C.Cl.CN(C)CCCC(N=C=N)C.Cl>ClCCl>[CH2:1]([O:8][C:9]1[CH:27]=[CH:26][C:25]([Br:28])=[CH:24][C:10]=1[CH2:11][N:12]([C:15]1[CH:20]=[CH:19][C:18]([C:21]([NH:35][S:32]([CH2:29][CH2:30][CH3:31])(=[O:34])=[O:33])=[O:23])=[CH:17][N:16]=1)[CH2:13][CH3:14])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1참가 물질
7
반응물 5
생성물 1
시약·촉매·용매 1
실험 절차
To a solution of 2-(N-(2-benzyloxy-5-bromobenzyl)-N-ethylamino]pyridine-5-carboxylic acid (0.89 g) in dichloromethane (50 ml) was added propanesulphonamide (0.3 g), dimethylaminopyrimidine (0.493 g) and 1-(3-dimethylaminopropyl)ethylcarbodiimide hydrochloride (0.58 g). The mixture was stirred at ambient temperature for 18 hours, and poured into 2N HCl. The organic layer was separated and washed with water and brine, then dried (MgSO4), filtered and evaporated. The resulting oil was purified by chromatography on silica gel (eluting with 5% ethylacetate/dichloromethane to give N-(2-[N-(2-benzyloxy-5-bromobenzyl)-N-ethylamino]pyridine-5-carbonyl)propanesulphonamide (271 mg) as a white foam.
후처리
- customThe organic layer was separated
- washwashed with water and brine
- dry with materialdried (MgSO4)
- filtrationfiltered
- customevaporated
- customThe resulting oil was purified by chromatography on silica gel (
- washeluting with 5% ethylacetate/dichloromethane
출처 및 근거
- ORD 기록
- ord-8c64db4ba7724ab8abb4c242bc02427f
- 출처 데이터셋
- uspto-grants-1998_12
- 특허 번호
- US05843942
연결된 노트
불러오는 중…