4-[(6-Chloropyridin-3-yl)sulfonyl]morpholine → HCID 136342138, 화합물
반응식
Cl[C:2]1[N:7]=[CH:6][C:5]([S:8]([N:11]2[CH2:16][CH2:15][O:14][CH2:13][CH2:12]2)(=[O:10])=[O:9])=[CH:4][CH:3]=1.[C:17]([C:19]1[CH:20]=[C:21]2[C:25](=[CH:26][CH:27]=1)[NH:24][C:23](=[O:28])[CH2:22]2)#[N:18]>>[OH:28][C:23]1[NH:24][C:25]2[C:21]([C:22]=1[C:2]1[CH:3]=[CH:4][C:5]([S:8]([N:11]3[CH2:16][CH2:15][O:14][CH2:13][CH2:12]3)(=[O:10])=[O:9])=[CH:6][N:7]=1)=[CH:20][C:19]([C:17]#[N:18])=[CH:27][CH:26]=2참가 물질
3
실험 절차
The title compound was prepared as described for Example 101 using 4-[(6-chloropyridin-3-yl)sulfonyl]morpholine and 5-cyanooxindole. The reaction mixture was quenched with water and the solvents were evaporated in vacuo. Water was added and the mixture was filtered. The solid material was washed with water, methanol, ethyl acetate and diethyl ether to give the title compound. Yield: 44%: MS (ES) m/z 385 (M++1).
후처리
- customThe title compound was prepared
- customThe reaction mixture was quenched with water
- customthe solvents were evaporated in vacuo
- additionWater was added