2,6-Dimethylmorpholine → HCID 25203979, compound

HRID 1710351Notes

Reaction equation

HRID 1710351 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.[CH3:26][CH:27]1[O:32][CH:31]([CH3:33])[CH2:30][NH:29][CH2:28]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:29]1[CH2:28][CH:27]([CH3:26])[O:32][CH:31]([CH3:33])[CH2:30]1)=[O:13])[CH2:8]2

Participants

3

Reactant 2

HCID 1108622,6-DimethylmorpholineHCID 575502625-chloro-1-phenyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide2×

Product 1

HCID 25203979HCID 25203979, compound

Procedure

5-(2,6-Dimethyl-morpholin-4-y1)-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 2,6-dimethylmorpholine. Mass spectrum (ES) MH+=435.

Sources & evidence

ORD record
ord-d4ad9563d3004515ae82680136e8a20b
Source dataset
uspto-grants-2010_09
Patent number
US07790711B2

Reaction notes

Loading…