2,6-Dichlorobenzoyl chloride → 5-Amino-N-(2-{[[(2,6-dichlorophenyl)carbonyl](methyl)amino]methyl}-3,3,3-trifluoro-2-hydroxypropyl)-1-(4-fluorophenyl)-1H-pyrazole-4-carboxamide
반응식
[NH2:1][C:2]1[N:6]([C:7]2[CH:12]=[CH:11][C:10]([F:13])=[CH:9][CH:8]=2)[N:5]=[CH:4][C:3]=1[C:14]([NH:16][CH2:17][C:18]([OH:26])([CH2:23][NH:24][CH3:25])[C:19]([F:22])([F:21])[F:20])=[O:15].C(N(C(C)C)CC)(C)C.[Cl:36][C:37]1[CH:45]=[CH:44][CH:43]=[C:42]([Cl:46])[C:38]=1[C:39](Cl)=[O:40]>O1CCCC1>[C:18]([O-:26])(=[O:40])[CH3:23].[NH2:1][C:2]1[N:6]([C:7]2[CH:8]=[CH:9][C:10]([F:13])=[CH:11][CH:12]=2)[N:5]=[CH:4][C:3]=1[C:14]([NH:16][CH2:17][C:18]([CH2:23][N:24]([C:39]([C:38]1[C:37]([Cl:36])=[CH:45][CH:44]=[CH:43][C:42]=1[Cl:46])=[O:40])[CH3:25])([OH:26])[C:19]([F:22])([F:21])[F:20])=[O:15]참가 물질
반응물 3
생성물 2
시약·촉매·용매 1
실험 절차
To a solution of 5-amino-1-(4-fluorophenyl)-N-{3,3,3-trifluoro-2-hydroxy-2-[(methylamino)methyl]propyl}-1H-pyrazole-4-carboxamide (56 mg, 0.15 mmol) in anhydrous tetrahydrofuran (2 ml) cooled in ice was added diisopropylethylamine (0.052 ml, 0.3 mmol) followed by 2,6-dichlorobenzoyl chloride (0.023 ml, 0.164 mmol). After 20 minutes, the mixture was removed from the ice and left at 21° C. for 19 hours. The mixture was blown down, the residue was dissolved in dichloromethane (3 ml) and washed with 2M hydrochloric acid (1 ml) and water (1 ml). It was again blown down and purified on a 5 g SPE cartridge, eluting with dichloromethane and then mixtures of cyclohexane/ethyl:acetate (10:1), (5:1), (3:1) and finally (2:1) to give the title compound (55.6 mg).
후처리
- customthe mixture was removed from the ice
- waitleft at 21° C. for 19 hours
- dissolutionthe residue was dissolved in dichloromethane (3 ml)
- washwashed with 2M hydrochloric acid (1 ml) and water (1 ml)
- custompurified on a 5 g SPE cartridge
- washeluting with dichloromethane
출처 및 근거
- ORD 기록
- ord-409c5855d36b4265bc02e23118123bea
- 출처 데이터셋
- uspto-grants-2012_08
- 특허 번호
- US08247377B2
반응 노트
불러오는 중…