Hydrochloric Acid → 4-({1-[2-(4-cyanophenyl)ethyl]-4-hydroxypiperidin-4-ylmethyl}methylamino)-N-hydroxybenzamide monohydrochloride
반응식
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][N:11]2[CH2:16][CH2:15][C:14]([CH2:18][N:19]([CH3:36])[C:20]3[CH:35]=[CH:34][C:23]([C:24]([NH:26][O:27]C4CCCCO4)=[O:25])=[CH:22][CH:21]=3)([OH:17])[CH2:13][CH2:12]2)=[CH:5][CH:4]=1)#[N:2].[ClH:37]>CO>[ClH:37].[C:1]([C:3]1[CH:4]=[CH:5][C:6]([CH2:9][CH2:10][N:11]2[CH2:16][CH2:15][C:14]([CH2:18][N:19]([CH3:36])[C:20]3[CH:21]=[CH:22][C:23]([C:24]([NH:26][OH:27])=[O:25])=[CH:34][CH:35]=3)([OH:17])[CH2:13][CH2:12]2)=[CH:7][CH:8]=1)#[N:2]참가 물질
4
반응물 2
생성물 1
시약·촉매·용매 1
실험 절차
To a solution of the compound (0.60 g) obtained in Example 23 in methanol (20 mL) was added 10% hydrogen chloride in methanol (5.0 mL), followed by stirring. The solvent was removed under reduced pressure, the residue was dissolved in methanol, and the solvent was removed again under reduced pressure. The residue was solidified with ethyl acetate, the resulting solid was finely powdered and was collected by filtration. The powder was dissolved in water (60 mL), and the solvent was removed under reduced pressure. The residue was finely powdered and dried under reduced pressure to yield the titled compound (447 mg) as a powder.
후처리
- customThe solvent was removed under reduced pressure
- dissolutionthe residue was dissolved in methanol
- customthe solvent was removed again under reduced pressure
- filtrationwas collected by filtration
- dissolutionThe powder was dissolved in water (60 mL)
- customthe solvent was removed under reduced pressure
- customdried under reduced pressure
출처 및 근거
- ORD 기록
- ord-2aeaeed88cf94e4481de9abd9f3919ce
- 출처 데이터셋
- uspto-grants-2009_02
- 특허 번호
- US07494987B2
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