1H-1,2,4-Triazole → HCID 11703358, compound

HRID 2069218Notes

Reaction equation

HRID 2069218 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]=[N: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]=[N:25][CH:24]=[N:23]1)([O-:14])=[O:13]

Participants

3

Reactant 2

HCID 92571H-1,2,4-TriazoleHCID 58964482N-(6-fluoro-7-nitro-2,4-dioxo-1,4-dihydro-2H-quinazolin-3-yl)-methanesulfonamide

Product 1

HCID 11703358HCID 11703358, compoundYield 83%

Procedure

N-(6-Fluoro-7-nitro-2,4-dioxo-1,4-dihydro-2H-quinazolin-3-yl)-methanesulfonamide (20 mg, 0.0628 mmol) is reacted with 1H-[1,2,4]triazole according to the GPB affording 19 mg (83%) of a yellowish powder. Rt=2.87 min.

Sources & evidence

ORD record
ord-af82b7e2d4ae414bbe1102c88b25294f
Source dataset
uspto-grants-2012_10
Patent number
US08299085B2

Reaction notes

Loading…