Sodium Bicarbonate → 3-[4-Hydroxy-4-(2-methyl-5-phenylpyrrol-1-yl)methyl-piperidino]methyl-1H-pyridin-2-one

HRID 606242노트

반응식

HRID 606242 반응식
[OH:1][C:2]1([CH2:8][N:9]2[C:13]([CH3:14])=[CH:12][CH:11]=[C:10]2[C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH2:7][CH2:6][NH:5][CH2:4][CH2:3]1.[O:21]=[C:22]1[C:27]([CH:28]=O)=[CH:26][CH:25]=[CH:24][NH:23]1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].C(=O)(O)[O-].[Na+]>ClCCl.C(Cl)(Cl)Cl.C(OCC)(=O)C.C(O)(=O)C>[OH:1][C:2]1([CH2:8][N:9]2[C:10]([C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)=[CH:11][CH:12]=[C:13]2[CH3:14])[CH2:7][CH2:6][N:5]([CH2:28][C:27]2[C:22](=[O:21])[NH:23][CH:24]=[CH:25][CH:26]=2)[CH2:4][CH2:3]1

참가 물질

9

실험 절차

After dissolving 35 mg of 4-hydroxy-4-(2-phenyl-5-methylpyrrol-1-yl)methyl-piperidine in 5 ml of dichloromethane, 16 mg of 2-oxo-1,2-dihydropyridine-3-carboxaldehyde and 0.02 ml of acetic acid were added and the mixture was stirred for 20 minutes at room temperature. Next, 41 mg of sodium triacetoxyborohydride was added and the mixture was stirred overnight at room temperature. Saturated aqueous sodium bicarbonate solution was added to the reaction mixture and extraction was performed with ethyl acetate and chloroform. After drying the organic layer over magnesium sulfate, the solvent was distilled off under reduced pressure. The obtained residue was purified by NH silica gel column chromatography to obtain the title compound (19 mg, 39% yield).

후처리

  1. additionwere added
  2. stirringthe mixture was stirred overnight at room temperature
  3. dry with materialAfter drying the organic layer over magnesium sulfate
  4. distillationthe solvent was distilled off under reduced pressure
  5. customThe obtained residue was purified by NH silica gel column chromatography

출처 및 근거

ORD 기록
ord-5ce58563647b4b8d9db1db8c63b1f794
출처 데이터셋
uspto-grants-2011_03
특허 번호
US07915274B2

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