6-(2,6-Dimethoxyphenyl)piperidin-2-one → 1-((6-(Difluoromethoxy)pyridin-3-yl)methyl)-6-(2,6-dimethoxyphenyl)piperidin-2-one

HRID 594595ノート

反応式

HRID 594595 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([O:9][CH3:10])[C:4]=1[CH:11]1[NH:16][C:15](=[O:17])[CH2:14][CH2:13][CH2:12]1.Br[CH2:19][C:20]1[CH:21]=[CH:22][C:23]([O:26][CH:27]([F:29])[F:28])=[N:24][CH:25]=1>>[F:29][CH:27]([F:28])[O:26][C:23]1[N:24]=[CH:25][C:20]([CH2:19][N:16]2[CH:11]([C:4]3[C:5]([O:9][CH3:10])=[CH:6][CH:7]=[CH:8][C:3]=3[O:2][CH3:1])[CH2:12][CH2:13][CH2:14][C:15]2=[O:17])=[CH:21][CH:22]=1

参加物

3

反応物 2

HCID 690825266-(2,6-Dimethoxyphenyl)piperidin-2-oneHCID 690853875-(Bromomethyl)-2-(difluoromethoxy)pyridine

生成物 1

HCID 690827151-((6-(Difluoromethoxy)pyridin-3-yl)methyl)-6-(2,6-dimethoxyphenyl)piperidin-2-one

実験手順

Prepared according to the described general procedure 4 (GP4) by reaction of 6-(2,6-dimethoxyphenyl)piperidin-2-one with 5-(bromomethyl)-2-(difluoromethoxy)pyridine. Subsequent purification by preparative HPLC afforded the target compound. LC-MS (conditions D): tR=1.03 min.; [M+H]+: 393.53 g/mol.

後処理

  1. customPrepared
  2. customSubsequent purification by preparative HPLC
  3. customafforded the target compound

出典と根拠

ORDレコード
ord-8f92ce179b77464dac3d8303e5bdeb81
出典データセット
uspto-grants-2016_01
特許番号
US09242970B2

反応ノート

読み込み中…