Benzylamine → HCID 11531544, compound
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].[CH2:22]([NH2:29])[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1>>[CH2:22]([NH:29][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])[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1Participants
3
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 benzylamine according to the GPA affording 8 mg (31%) of a red powder. Rt=3.45 min.
Sources & evidence
- ORD record
- ord-66e4689a825745ca8f0c025d75a727a4
- Source dataset
- uspto-grants-2012_10
- Patent number
- US08299085B2
Reaction notes
Loading…