Sodium Bicarbonate → 3-[4-Hydroxy-4-[(2-fluorophenyl)ethynyl)piperidino]methyl-1H-pyridin-2-one

HRID 914898노트

반응식

HRID 914898 반응식
Cl.[OH:2][C:3]1([C:9]#[C:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=2[F:17])[CH2:8][CH2:7][NH:6][CH2:5][CH2:4]1.[O:18]=[C:19]1[C:24]([CH:25]=O)=[CH:23][CH:22]=[CH:21][NH:20]1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].C(=O)(O)[O-].[Na+]>C(OCC)(=O)C.ClCCl>[OH:2][C:3]1([C:9]#[C:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=2[F:17])[CH2:4][CH2:5][N:6]([CH2:25][C:24]2[C:19](=[O:18])[NH:20][CH:21]=[CH:22][CH:23]=2)[CH2:7][CH2:8]1

참가 물질

7

실험 절차

After then adding 253 mg of the 4-hydroxy-4-[(2-fluorophenyl)ethynyl]piperidine hydrochloride to 10 ml of dichloromethane, 158 mg of 2-oxo-1,2-dihydropyridine-3-carboxaldehyde was added and the mixture was stirred for 10 minutes at room temperature. Next, 315 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. After drying the organic layer over magnesium sulfate, the solvent was distilled off under reduced pressure. The residue was purified by NH silica gel column chromatography to obtain the title compound (32 mg, 10% yield).

후처리

  1. additionwas 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 residue was purified by NH silica gel column chromatography

출처 및 근거

ORD 기록
ord-6062b52183ae45c78b642ab9c88d928b
출처 데이터셋
uspto-grants-2007_09
특허 번호
US07265108B2

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