Acetyl chloride → Methyl 3-(1-acetylpiperidin-2-yl)-5-(1-cyclohexylethyl)benzoate
反応式
[C:1]1([C:7]([C:9]2[CH:10]=[C:11]([CH:16]=[C:17]([C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][N:20]=3)[CH:18]=2)[C:12]([O:14][CH3:15])=[O:13])=[CH2:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.CCN(C(C)C)C(C)C.[C:34](Cl)(=[O:36])[CH3:35]>C(O)C.Cl.C(Cl)Cl.O=[Pt]=O>[C:34]([N:20]1[CH2:21][CH2:22][CH2:23][CH2:24][CH:19]1[C:17]1[CH:16]=[C:11]([CH:10]=[C:9]([CH:7]([CH:1]2[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]2)[CH3:8])[CH:18]=1)[C:12]([O:14][CH3:15])=[O:13])(=[O:36])[CH3:35]参加物
実験手順
To an argon purged solution of methyl 3-(1-phenylvinyl)-5-(pyridin-2-yl)benzoate (73 mg, 0.23 mmol) in ethanol (5 mL) and HCl (conc. 1 mL) was added PtO2 (7 mg, 0.023 mmol). The mixture was hydrogenated under a hydrogen atmosphere (35 psi) for 6 h. The reaction mixture was purged with argon, filtered through a 0.2 μm filter, and concentrated. The resulting crude material was taken up with CH2Cl2 (5 mL) after which iPr2NEt (0.1 mL, 0.58 mmol) and acetyl chloride (18 μL, 0.25 mmol) were successively added. The mixture was stirred for 30 min, then diluted with CH2Cl2 (30 mL) and washed successively with 0.5 M HCl (1×10 mL), 9% sodium carbonate (1×10 mL), brine, dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude residue containing the title compound was used without further purification. MS m/z=372 [M+1]+; Calc'd for C23H33NO3: 371.
後処理
- customfor 6 h
- customThe reaction mixture was purged with argon
- filtrationfiltered through a 0.2 μm
- filtrationfilter
- concentrationconcentrated
- additionwere successively added
- washwashed successively with 0.5 M HCl (1×10 mL), 9% sodium carbonate (1×10 mL), brine
- dry with materialdried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- additionThe crude residue containing the title compound
- customwas used without further purification
出典と根拠
- ORDレコード
- ord-1e9e9eee4ea24d09a4ceddc83fbd9b55
- 出典データセット
- uspto-grants-2010_11
- 特許番号
- US07838676B2
反応ノート
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