2-(Bromomethyl)-5-chlorobenzonitrile → HCID 68662509, 화합물
반응식
[NH2:1][C:2]1[N:10]=[CH:9][C:8]([Cl:11])=[CH:7][C:3]=1[C:4]([NH2:6])=[O:5].Br[CH2:13][C:14]1[CH:21]=[CH:20][C:19]([Cl:22])=[CH:18][C:15]=1[C:16]#[N:17]>CN(C)C=O>[ClH:11].[Cl:11][C:8]1[CH:7]=[C:3]([C:4]([NH2:6])=[O:5])[C:2](=[NH:1])[N:10]([CH2:13][C:14]2[CH:21]=[CH:20][C:19]([Cl:22])=[CH:18][C:15]=2[C:16]#[N:17])[CH:9]=1참가 물질
반응 조건
- 온도
- 100 °C
실험 절차
To a solution of 2-amino-5-chloronicotinamide (0.16 g) in N,N-dimethylformamide (3 ml) was added 2-(bromomethyl)-5-chlorobenzonitrile (0.32 g), and the mixture was stirred at 100° C. for 14 hr. The reaction mixture was quenched with saturated aqueous sodium hydrogen carbonate solution and extracted with ethyl acetate. The extract was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel chromatography (ethyl acetate:hexane=3:2-4:1). 2N Hydrochloric acid-methanol solution (1 ml) was added to the obtained yellow oil at room temperature, and the obtained precipitate was recrystallized from methanol-ethyl acetate to give the title compound (3 mg).
후처리
- customThe reaction mixture was quenched with saturated aqueous sodium hydrogen carbonate solution
- extractionextracted with ethyl acetate
- washThe extract was washed with saturated brine
- dry with materialdried over anhydrous magnesium sulfate
- customThe solvent was evaporated under reduced pressure
- customthe obtained residue was purified by silica gel chromatography (ethyl acetate:hexane=3:2-4:1)
- addition2N Hydrochloric acid-methanol solution (1 ml) was added to the obtained yellow oil at room temperature
- customthe obtained precipitate was recrystallized from methanol-ethyl acetate
출처 및 근거
- ORD 기록
- ord-675aab9ae4bd40c69e955e0f7cf1e7f6
- 출처 데이터셋
- uspto-grants-2013_06
- 특허 번호
- US08470859B2
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