Sodium hydride → 4-(2,6-Dimethyl-4-(pyridin-4-yl)phenoxy)-6-chloro-1H-pyrazolo[3,4-d]pyrimidine
반응식
[H-].[Na+].[CH3:3][C:4]1[CH:9]=[C:8]([C:10]2[CH:15]=[CH:14][N:13]=[CH:12][CH:11]=2)[CH:7]=[C:6]([CH3:16])[C:5]=1[OH:17].Cl[C:19]1[N:24]=[C:23]([Cl:25])[N:22]=[C:21]2[NH:26][N:27]=[CH:28][C:20]=12>>[CH3:3][C:4]1[CH:9]=[C:8]([C:10]2[CH:11]=[CH:12][N:13]=[CH:14][CH:15]=2)[CH:7]=[C:6]([CH3:16])[C:5]=1[O:17][C:19]1[N:24]=[C:23]([Cl:25])[N:22]=[C:21]2[NH:26][N:27]=[CH:28][C:20]=12참가 물질
4
실험 절차
Sodium hydride (1.2 eq) is added to 2,6-dimethyl-4-(pyridin-4-yl)phenol (prepared according to literature procedures, see Combellas et al., Tetrahedron Letters, 1992, 33, 4923) (1.2 eq) in 1-methyl-2-pyrridone (2 ml/mmol) at 0° C. The reaction mixture is stirred at room temperature for 30 min and a solution of 4,6-dichloro-1H-pyrazolo[3,4-d]pyrimidine (1 eq) in 1-methyl-2-pyrridone (1 ml/mmol) is added. The resulting mixture is heated to 100° C. for 16 h, cooled to room temperature, poured into ice water and extracted with CHCl3 (×3). The combined organic layers are washed with water and brine, dried (Na2SO4), concentrated to dryness and purified by silica gel chromatography.
후처리
- temperatureThe resulting mixture is heated to 100° C. for 16 h
- temperaturecooled to room temperature
- extractionextracted with CHCl3 (×3)
- washThe combined organic layers are washed with water and brine
- dry with materialdried (Na2SO4)
- concentrationconcentrated to dryness
- custompurified by silica gel chromatography
출처 및 근거
- ORD 기록
- ord-13b350c4af244183a627858341013c9b
- 출처 데이터셋
- uspto-grants-2012_06
- 특허 번호
- US08207178B2
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