Sodium hydride → 5-Chloro-6-((4'-fluoro spiro[benzo[d][1,3]dioxole-2,1'-cyclohexane]-4'-yl)methoxy)pyridine-3-sulfonamide
반응식
[F:1][C:2]1([CH2:16][OH:17])[CH2:7][CH2:6][C:5]2([O:11][C:10]3[CH:12]=[CH:13][CH:14]=[CH:15][C:9]=3[O:8]2)[CH2:4][CH2:3]1.[H-].[Na+].[Cl:20][C:21]1[CH:22]=[C:23]([S:28]([NH2:31])(=[O:30])=[O:29])[CH:24]=[N:25][C:26]=1Cl.[NH4+].[Cl-]>CN(C)C=O>[Cl:20][C:21]1[CH:22]=[C:23]([S:28]([NH2:31])(=[O:30])=[O:29])[CH:24]=[N:25][C:26]=1[O:17][CH2:16][C:2]1([F:1])[CH2:3][CH2:4][C:5]2([O:8][C:9]3[CH:15]=[CH:14][CH:13]=[CH:12][C:10]=3[O:11]2)[CH2:6][CH2:7]1참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
To a solution of EXAMPLE 350C (89 mg) in N,N-dimethylformamide (3 mL) was added NaH (65% in mineral oil, 36 mg). The mixture was stirred for 30 minutes, and then 5,6-dichloropyridine-3-sulfonamide (85 mg) was added. The mixture was stirred overnight. The mixture was poured over aqueous NH4Cl and extracted with ethyl acetate (100 mL). The combined organic layers were washed with water, brine and dried over Na2SO4. After filtration and evaporation of the solvent, the residue was loaded on a silica gel cartridge and eluted with 30% ethyl acetate in hexane to provide the title compound.
후처리
- stirringThe mixture was stirred overnight
- extractionextracted with ethyl acetate (100 mL)
- washThe combined organic layers were washed with water, brine
- dry with materialdried over Na2SO4
- filtrationAfter filtration and evaporation of the solvent
- washeluted with 30% ethyl acetate in hexane
출처 및 근거
- ORD 기록
- ord-f5393e1e1e4b4b0881c775b51a46e559
- 출처 데이터셋
- uspto-grants-2013_10
- 특허 번호
- US08546399B2
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