Sodium Bicarbonate → 1-(2-Oxo-1,2-dihydro-3-pyridylmethyl)-4-(2-methylphenoxymethyl)piperidine-4-carbonitrile

HRID 890089ノート

反応式

HRID 890089 の反応式
Cl.[C:2]([C:4]1([CH2:10][O:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[CH3:18])[CH2:9][CH2:8][NH:7][CH2:6][CH2:5]1)#[N:3].[O:19]=[C:20]1[C:25]([CH:26]=O)=[CH:24][CH:23]=[CH:22][NH:21]1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].C(=O)(O)[O-].[Na+]>C(Cl)(Cl)Cl.C(OCC)(=O)C.ClCCl>[O:19]=[C:20]1[C:25]([CH2:26][N:7]2[CH2:8][CH2:9][C:4]([CH2:10][O:11][C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=3[CH3:18])([C:2]#[N:3])[CH2:5][CH2:6]2)=[CH:24][CH:23]=[CH:22][NH:21]1

参加物

8

実験手順

After then adding 117 mg of the 4-cyano-4-(2-methylphenoxymethyl)piperidine hydrochloride and 70 mg of 2-oxo-1,2-dihydropyridine-3-carboxaldehyde [CAS No.36404-89-4] to 10 ml of dichloromethane, the mixture was stirred for 20 minutes at room temperature. 139 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 (solvent: chloroform/methanol) to obtain the title compound (7 mg, 5% yield).

後処理

  1. dry with materialAfter drying the organic layer over magnesium sulfate
  2. distillationthe solvent was distilled off under reduced pressure
  3. customThe obtained residue was purified by NH silica gel column chromatography (solvent: chloroform/methanol)

出典と根拠

ORDレコード
ord-1a4542b600d648cc9fd77c99e36d9cdd
出典データセット
uspto-grants-2006_02
特許番号
US06995144B2

反応ノート

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