1-Methyl-1H-pyrazole-4-carboxylic acid → HCID 71217341, compound
Reaction equation
[NH2:1][CH2:2][C:3]1[C:12](=[O:13])[C:11]2[C:6](=[CH:7][C:8]([Cl:14])=[CH:9][CH:10]=2)[N:5]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH:4]=1.[CH3:21][N:22]1[CH:26]=[C:25]([C:27](O)=[O:28])[CH:24]=[N:23]1>>[Cl:14][C:8]1[CH:7]=[C:6]2[C:11]([C:12](=[O:13])[C:3]([CH2:2][NH:1][C:27]([C:25]3[CH:24]=[N:23][N:22]([CH3:21])[CH:26]=3)=[O:28])=[CH:4][N:5]2[C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=2)=[CH:10][CH:9]=1Participants
3
Procedure
Methyl-1H-pyrazole-4-carboxylic acid (7-chloro-4-oxo-1-phenyl-1,4-dihydro-quinolin-3-ylmethyl)-amide was prepared starting from intermediate D and 1-methyl-1H-pyrazole-4-carboxylic acid. MS calcd. for C21H18ClN4O2 [(M+H)+] 393.1, obsd. 393.0.
Sources & evidence
- ORD record
- ord-22462cbf3633449798d655f6add91afe
- Source dataset
- uspto-grants-2013_08
- Patent number
- US08501732B2
Reaction notes
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