Hydrochloric Acid → N-{3-[(4-Cyano-1H-pyrrolo[2,3-b]pyridin-3-yl)-hydroxy-methyl]-2,4-difluoro-phenyl}-4-trifluoromethyl-benzenesulfonamide
반응식
[NH:1]1[C:5]2[N:6]=[CH:7][CH:8]=[C:9]([C:10]#[N:11])[C:4]=2[CH:3]=[CH:2]1.[F:12][C:13]1[C:18]([CH:19]=[O:20])=[C:17]([F:21])[CH:16]=[CH:15][C:14]=1[NH:22][S:23]([C:26]1[CH:31]=[CH:30][C:29]([C:32]([F:35])([F:34])[F:33])=[CH:28][CH:27]=1)(=[O:25])=[O:24].[OH-].[K+].Cl>CO>[C:10]([C:9]1[CH:8]=[CH:7][N:6]=[C:5]2[NH:1][CH:2]=[C:3]([CH:19]([OH:20])[C:18]3[C:13]([F:12])=[C:14]([NH:22][S:23]([C:26]4[CH:27]=[CH:28][C:29]([C:32]([F:35])([F:34])[F:33])=[CH:30][CH:31]=4)(=[O:25])=[O:24])[CH:15]=[CH:16][C:17]=3[F:21])[C:4]=12)#[N:11]참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
Into a round bottom flask 1H-pyrrolo[2,3-b]pyridine-4-carbonitrile (5, 0.054 g, 0.38 mmol), N-(2,4-difluoro-3-formyl-phenyl)-4-trifluoromethyl-benzenesulfonamide (4, 0.179 g, 0.49 mmol), 0.75 mL of methanol and potassium hydroxide (0.103 g, 1.89 mmol) were combined. The reaction was stirred at room temperature for 46 hours, then neutralized with 0.1 N aqueous hydrochloric acid and extracted 3× with ethyl acetate. The organic layers were combined and washed with brine, then dried over sodium sulfate, filtered and the filtrate concentrated under vacuum. The material was purified by silica gel column chromatography eluting with ethyl acetate and hexane. The appropriate fractions were combined and the solvent removed under vacuum to provide the desired compound (6, 0.018 g). MS (ESI) [M+H+]+=509.1.
후처리
- extractionextracted 3× with ethyl acetate
- washwashed with brine
- dry with materialdried over sodium sulfate
- filtrationfiltered
- concentrationthe filtrate concentrated under vacuum
- customThe material was purified by silica gel column chromatography
- washeluting with ethyl acetate and hexane
- customthe solvent removed under vacuum
출처 및 근거
- ORD 기록
- ord-fd599e8bf30043eeaf150f9de6cdc22f
- 출처 데이터셋
- uspto-grants-2012_03
- 특허 번호
- US08129404B2
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