N-Methylbenzeneethanamine → 5-(Methyl-phenethyl-amino)-1-phenyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide

HRID 1710350

反応式

HRID 1710350 の反応式
[CH:1]12[CH2:10][CH:5]3[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]3)[CH:2]1[NH:11][C:12]([C:14]1[CH:15]=[N:16][N:17]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[C:18]=1Cl)=[O:13])[CH2:8]2.[CH3:26][NH:27][CH2:28][CH2:29][C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1>>[CH:1]12[CH2:10][CH:5]3[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]3)[CH:2]1[NH:11][C:12]([C:14]1[CH:15]=[N:16][N:17]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[C:18]=1[N:27]([CH3:26])[CH2:28][CH2:29][C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1)=[O:13])[CH2:8]2

参加物

3

反応物 2

HCID 11503N-MethylbenzeneethanamineHCID 575502625-chloro-1-phenyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide2 回

生成物 1

HCID 252050105-(Methyl-phenethyl-amino)-1-phenyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide

実験手順

5-(Methyl-phenethyl-amino)-1-phenyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide was prepared using Procedure A from 5-chloro-1-phenyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide (Intermediate 3) and N-methylphenethylamine. Mass spectrum (ES) MH+=455.

出典と根拠

ORDレコード
ord-d106877c4ea34d7aa515297822defbff
出典データセット
uspto-grants-2010_09
特許番号
US07790711B2

関連ノート

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