1-(3,4-Difluorobenzyl)-2-oxo-1,2-dihydropyridine-3-carbonyl chloride → N-(3-(4-chloro-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)benzyl)-1-(3,4-difluorobenzyl)-2-oxo-1,2-dihydropyridine-3-carboxamide
반응식
[Cl:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]2[N:8]([S:19]([C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)(=[O:21])=[O:20])[CH:9]=[C:10]([C:11]3[CH:12]=[C:13]([CH2:17][NH2:18])[CH:14]=[CH:15][CH:16]=3)[C:3]=12.[F:28][C:29]1[CH:30]=[C:31]([CH:43]=[CH:44][C:45]=1[F:46])[CH2:32][N:33]1[CH:38]=[CH:37][CH:36]=[C:35]([C:39](Cl)=[O:40])[C:34]1=[O:42]>C(Cl)Cl>[Cl:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]2[N:8]([S:19]([C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)(=[O:21])=[O:20])[CH:9]=[C:10]([C:11]3[CH:12]=[C:13]([CH:14]=[CH:15][CH:16]=3)[CH2:17][NH:18][C:39]([C:35]3[C:34](=[O:42])[N:33]([CH2:32][C:31]4[CH:43]=[CH:44][C:45]([F:46])=[C:29]([F:28])[CH:30]=4)[CH:38]=[CH:37][CH:36]=3)=[O:40])[C:3]=12참가 물질
4
반응물 2
생성물 1
시약·촉매·용매 1
실험 절차
43 mg of (3-(4-chloro-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)phenyl)methanamine, 32 mg of crude 1-(3,4-difluorobenzyl)-2-oxo-1,2-dihydropyridine-3-carbonyl chloride were dissolved in DCM, TEA was added, then the resulted mixture was stirred at room temperature for overnight. The solvent was removed on a rotary evaporator and the crude was purified by chromatography to give 32 mg of N-(3-(4-chloro-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)benzyl)-1-(3,4-difluorobenzyl)-2-oxo-1,2-dihydropyridine-3-carboxamide, yield: 50%.
후처리
- additionTEA was added
- customThe solvent was removed on a rotary evaporator
- customthe crude was purified by chromatography
출처 및 근거
- ORD 기록
- ord-5823c1c95459401e87f46913eaf3dc21
- 출처 데이터셋
- uspto-grants-2014_07
- 특허 번호
- US08778977B2
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