Dimethylcarbamoyl Chloride → 2-(2,4-difluorophenyl)-3-(6-cyanopyrimidin-4-yl)-1-(1H-1,2,4-triazol-1-yl)butan-2-ol
반응식
[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[C:9]([OH:25])([CH:16]([C:18]1[CH:23]=[CH:22][N+:21]([O-])=[CH:20][N:19]=1)[CH3:17])[CH2:10][N:11]1[CH:15]=[N:14][CH:13]=[N:12]1.[CH3:26][N:27](C)C(Cl)=O.C[Si](C#N)(C)C>ClCCl>[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[C:9]([OH:25])([CH:16]([C:18]1[CH:23]=[C:22]([C:26]#[N:27])[N:21]=[CH:20][N:19]=1)[CH3:17])[CH2:10][N:11]1[CH:15]=[N:14][CH:13]=[N:12]1참가 물질
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
A mixture of the product of part (i) (0.80 g) and N,N-dimethylcarbamoyl chloride (0.50 g) in dichloromethane (10 ml) was stirred at room temperature for 2 hours. Trimethylsilyl cyanide (0.50 g) was added and stirring was continued for a further 6 days. The solution was evaporated and the residue was chromatographed on silica gel. Elution with dichloromethane/methanol (100:1) gave a product which was rechromatographed on silica gel. Elution was commenced with ether and the polarity of the eluant was gradually increased by the addition of up to 6% (by volume) of methanol. Combination and evaporation of the initial product-containing fractions gave 2-(2,4-difluorophenyl)-3-(6-cyanopyrimidin-4-yl)-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, (30 mg), m.p. 148°-149°.
후처리
- stirringstirring
- waitwas continued for a further 6 days
- customThe solution was evaporated
- customthe residue was chromatographed on silica gel
- washElution with dichloromethane/methanol (100:1)
- customgave a product which
- customwas rechromatographed on silica gel
- washElution
- temperaturethe polarity of the eluant was gradually increased by the addition of up to 6% (by volume) of methanol
- customCombination and evaporation of the
- additioninitial product-containing fractions
출처 및 근거
- ORD 기록
- ord-df2fc41b01f94dda96f8ff56bf233c95
- 출처 데이터셋
- uspto-grants-1992_05
- 특허 번호
- US05116844
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