Pyrazole → HCID 11624794, compound

HRID 2069221Notes

Reaction equation

HRID 2069221 reaction equation
F[C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[N+:12]([O-:14])=[O:13])[NH:8][C:7](=[O:15])[N:6]([NH:16][S:17]([CH3:20])(=[O:19])=[O:18])[C:5]2=[O:21].[NH:22]1[CH:26]=[CH:25][CH:24]=[N:23]1>>[N+:12]([C:11]1[CH:10]=[C:9]2[C:4]([C:5](=[O:21])[N:6]([NH:16][S:17]([CH3:20])(=[O:19])=[O:18])[C:7](=[O:15])[NH:8]2)=[CH:3][C:2]=1[N:22]1[CH:26]=[CH:25][CH:24]=[N:23]1)([O-:14])=[O:13]

Participants

3

Procedure

N-(6-Fluoro-7-nitro-2,4-dioxo-1,4-dihydro-2H-quinazolin-3-yl)-methanesulfonamide (30 mg, 0.0943 mmol) is reacted with 1H-pyrazole according to the GPB affording 9.4 mg (27%) of a red powder. Rt=3.64 min.

Sources & evidence

ORD record
ord-9249c00a04014f12a098d9f31a0eaf69
Source dataset
uspto-grants-2012_10
Patent number
US08299085B2

Reaction notes

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