N-(6-fluoro-7-nitro-2,4-dioxo-1,4-dihydro-2H-quinazolin-3-yl)-methanesulfonamide → HCID 11545913, compound

HRID 2069254Notes

Reaction equation

HRID 2069254 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]=[C:25]([CH2:27][C:28]#[N:29])[N:24]=[CH:23]1>>[C:28]([CH2:27][C:25]1[N:24]=[CH:23][N:22]([C:2]2[CH:3]=[C:4]3[C:9](=[CH:10][C:11]=2[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]3=[O:21])[CH:26]=1)#[N:29]

Participants

3

Reactant 2

HCID 58964482N-(6-fluoro-7-nitro-2,4-dioxo-1,4-dihydro-2H-quinazolin-3-yl)-methanesulfonamideHCID 178510863HCID 178510863, compound

Product 1

HCID 11545913HCID 11545913, compoundYield 47%

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-imidazol-4-yl)-acetonitrile according to the GPB affording 18.5 mg (47%) of a yellow powder. Rt=2.56 min.

Sources & evidence

ORD record
ord-f3da5f1a70c14470bae2af50ea55c88f
Source dataset
uspto-grants-2012_10
Patent number
US08299085B2

Reaction notes

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