4-Fluorobenzoic Acid → HCID 16722749, compound
Reaction equation
[CH3:1][C:2]1[O:6][N:5]=[C:4]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[C:3]=1[C:13]([NH:15][NH2:16])=[O:14].[F:17][C:18]1[CH:26]=[CH:25][C:21]([C:22](O)=O)=[CH:20][CH:19]=1>>[F:17][C:18]1[CH:26]=[CH:25][C:21]([C:22]2[O:14][C:13]([C:3]3[C:4]([C:7]4[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=4)=[N:5][O:6][C:2]=3[CH3:1])=[N:15][N:16]=2)=[CH:20][CH:19]=1Participants
3
Procedure
As described for example 2, 5-methyl-3-phenyl-isoxazole-4-carboxylic acid hydrazide (5.00 g, 23.0 mmol) was converted using 4-fluorobenzoic acid instead of o-toluic acid to the title compound (recrystallisation from tert-butylmethylether, 2.98 g, 40%) which was obtained as an off-white solid. MS: m/e=322.2 [M+H]+.
Sources & evidence
- ORD record
- ord-2100e47283ad48fb8364ee1f5d53fe13
- Source dataset
- uspto-grants-2009_06
- Patent number
- US07541372B2
Reaction notes
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