1-(4-(4-(aminomethyl)-1H-imidazol-1-yl)phenyl)pyridin-2(1H)-one hydrochloride → 1-(4-(4-(aminomethyl)-1H-imidazol-1-yl)phenyl)piperidin-2-one

HRID 2357838ノート

反応式

HRID 2357838 の反応式
Cl.[NH2:2][CH2:3][C:4]1[N:5]=[CH:6][N:7]([C:9]2[CH:14]=[CH:13][C:12]([N:15]3[CH:20]=[CH:19][CH:18]=[CH:17][C:16]3=[O:21])=[CH:11][CH:10]=2)[CH:8]=1>CO.[Pd]>[NH2:2][CH2:3][C:4]1[N:5]=[CH:6][N:7]([C:9]2[CH:10]=[CH:11][C:12]([N:15]3[CH2:20][CH2:19][CH2:18][CH2:17][C:16]3=[O:21])=[CH:13][CH:14]=2)[CH:8]=1

参加物

4

反応物 1

HCID 669741011-(4-(4-(aminomethyl)-1H-imidazol-1-yl)phenyl)pyridin-2(1H)-one hydrochloride

生成物 1

HCID 669740921-(4-(4-(aminomethyl)-1H-imidazol-1-yl)phenyl)piperidin-2-one収率 99.9%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

実験手順

A mixture of 1-(4-(4-(aminomethyl)-1H-imidazol-1-yl)phenyl)pyridin-2(1H)-one hydrochloride (60 mg, 0.20 mmol) and Pd—C (10%, 31 mg) in MeOH (6 mL) was hydrogenated under balloon H2 overnight. It was then filtered through celite. The filtrate was concentrated in vacuo to give 1-(4-(4-(aminomethyl)-1H-imidazol-1-yl)phenyl)piperidin-2-one (54 mg).

後処理

  1. customwas hydrogenated under balloon H2 overnight
  2. filtrationIt was then filtered through celite
  3. concentrationThe filtrate was concentrated in vacuo

出典と根拠

ORDレコード
ord-e9eddf41a39b4c97a69b54a6bc13052b
出典データセット
uspto-grants-2010_07
特許番号
US07763608B2

反応ノート

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