Acetamidine monohydrochloride → 10-Fluoro-5,7-dihydro-2-methyl-6h-pyrimido[5,4-d][1]benzazepin-6-one
Reaction equation
CN([CH:4]=[C:5]1[C:11](=O)[C:10]2[CH:13]=[C:14]([F:17])[CH:15]=[CH:16][C:9]=2[NH:8][C:7](=[O:18])[CH2:6]1)C.Cl.[C:20]([NH2:23])(=[NH:22])[CH3:21]>>[F:17][C:14]1[CH:15]=[CH:16][C:9]2[NH:8][C:7](=[O:18])[CH2:6][C:5]3[CH:4]=[N:22][C:20]([CH3:21])=[N:23][C:11]=3[C:10]=2[CH:13]=1Participants
3
Procedure
Analogous to Scheme 1, from 4-[(dimethylamino)methylene]-7-fluoro-3,4-dihydro-1H-benzazepine-2,5-dione and acetamidine hydrochloride. Yield: 50%.
Sources & evidence
- ORD record
- ord-95487d93e84f4a20976fb34b46cf20ec
- Source dataset
- uspto-grants-2004_02
- Patent number
- US06686352B2
Reaction notes
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