Cyclopropanecarboximidamide hydrochloride → HCID 23440997, compound
Reaction equation
CN([CH:4]=[C:5]1[C:11](=O)[C:10]2[CH:13]=[C:14]([CH3:17])[CH:15]=[CH:16][C:9]=2[NH:8][C:7](=[O:18])[CH2:6]1)C.Cl.[CH:20]1([C:23]([NH2:25])=[NH:24])[CH2:22][CH2:21]1>>[CH:20]1([C:23]2[N:24]=[CH:4][C:5]3[CH2:6][C:7](=[O:18])[NH:8][C:9]4[CH:16]=[CH:15][C:14]([CH3:17])=[CH:13][C:10]=4[C:11]=3[N:25]=2)[CH2:22][CH2:21]1Participants
3
Procedure
Analogous to Scheme 1, from 4-[(dimethylamino)methylene]-3,4-dihydro-7-methyl-1H-benzazepine-2,5-dione and cyclopropanecarboxamidine hydrochloride. Yield: 88%.
Sources & evidence
- ORD record
- ord-0ba4360a48374de9aba81165d0fbfc4c
- Source dataset
- uspto-grants-2004_02
- Patent number
- US06686352B2
Reaction notes
Loading…