Acetyl chloride → 1-[8-Chloro-1-(3,4,5,6-tetrahydro-2h-[1,2']bipyridinyl-4-yl)-4h,6h-2,3,5,10b-tetraaza-benzo[e]azulen-5-yl]-ethanone dihydrochloride
반응식
[C:1]([Cl:4])(=[O:3])[CH3:2].[Cl:5][C:6]1[CH:31]=[CH:30][C:9]2[N:10]3[C:14]([CH2:15][NH:16][CH2:17][C:8]=2[CH:7]=1)=[N:13][N:12]=[C:11]3[CH:18]1[CH2:23][CH2:22][N:21]([C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][N:25]=2)[CH2:20][CH2:19]1>ClCCl>[ClH:4].[ClH:5].[Cl:5][C:6]1[CH:31]=[CH:30][C:9]2[N:10]3[C:14]([CH2:15][N:16]([C:1](=[O:3])[CH3:2])[CH2:17][C:8]=2[CH:7]=1)=[N:13][N:12]=[C:11]3[CH:18]1[CH2:19][CH2:20][N:21]([C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][N:25]=2)[CH2:22][CH2:23]1참가 물질
4
반응물 2
생성물 1
시약·촉매·용매 1
실험 절차
Acetyl chloride (0.1 ml, 1.4 mmol) was added to an ice cooled solution of the amine of example 4 (200 mg, 0.53 mmol) in dichloromethane (5 ml) and stirred at room temperature for 20 hours. Dichloromethane was evaporated off under reduced pressure and the residue purified by chromatography on silica gel using methanol in dichloromethane (5:95) as eluant. The residue was dissolved in dichloromethane (2 ml) and hydrochloric acid (1M in diethyl ether, 2 ml) was added, and the solvents evaporated under reduced pressure to give the title compound as a brown foam (110 mg).
후처리
- customDichloromethane was evaporated off under reduced pressure
- customthe residue purified by chromatography on silica gel
- dissolutionThe residue was dissolved in dichloromethane (2 ml)
- additionhydrochloric acid (1M in diethyl ether, 2 ml) was added
- customthe solvents evaporated under reduced pressure
출처 및 근거
- ORD 기록
- ord-bf4b3aff5c8140f6a6ebdcc32bee5724
- 출처 데이터셋
- uspto-grants-2006_10
- 특허 번호
- US07119088B2
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