Cyclobutylamine → 5-Cyclobutylamino-1-phenyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide

HRID 1710345Notes

Reaction equation

HRID 1710345 reaction equation
[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.[CH:26]1([NH2:30])[CH2:29][CH2:28][CH2:27]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[NH:30][CH:26]1[CH2:29][CH2:28][CH2:27]1)=[O:13])[CH2:8]2

Participants

3

Reactant 2

HCID 75645CyclobutylamineHCID 575502625-chloro-1-phenyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide2×

Product 1

HCID 252050055-Cyclobutylamino-1-phenyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide

Procedure

5-Cyclobutylamino-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 cyclobutylamine. Mass spectrum (ES) MH+=391.

Sources & evidence

ORD record
ord-2eea2dbb9b93479e963b376b993e4b27
Source dataset
uspto-grants-2010_09
Patent number
US07790711B2

Reaction notes

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