Cyclopropylamine → HCID 11717353, 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].[CH:22]1([NH2:25])[CH2:24][CH2:23]1>>[CH:22]1([NH:25][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])[CH2:24][CH2:23]1Participants
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 cyclopropylamine according to the GPA affording 10 mg (31%) of a red powder. Rt=3.15 min.
Sources & evidence
- ORD record
- ord-7076593011f04785bc44b5ce5ec6a7ae
- Source dataset
- uspto-grants-2012_10
- Patent number
- US08299085B2
Reaction notes
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