[4-(4-Acetylpiperazin-1-yl)-3-methylphenyl]amine → 4-(4-Acetyl-1,4-diazepan-1-yl)aniline
Reaction equation
C(N1CCN(C2C=CC(N)=CC=2C)CC1)(=O)C.[C:18]([N:21]1[CH2:27][CH2:26][CH2:25][N:24]([C:28]2[CH:33]=[CH:32][C:31]([N+:34]([O-])=O)=[CH:30][CH:29]=2)[CH2:23][CH2:22]1)(=[O:20])[CH3:19]>>[C:18]([N:21]1[CH2:27][CH2:26][CH2:25][N:24]([C:28]2[CH:33]=[CH:32][C:31]([NH2:34])=[CH:30][CH:29]=2)[CH2:23][CH2:22]1)(=[O:20])[CH3:19]Participants
3
Procedure
Following the general procedure of Intermediate 36 but using 1-acetyl-4-(4-nitrophenyl)-1,4-diazepane (Intermediate 70) as starting material there was thus obtained the title compound in 97% yield; 1H NMR δ: 6.55-6.46 (4H, m), 4.30 (2H, br s), 3.59-3.48 (3H, m), 3.41-3.26 (5H, m), 1.99-1.72 (5H, m); MS m/e MH+: 234.
Sources & evidence
- ORD record
- ord-7ba91c56af9c40caa17de76e0ea347bb
- Source dataset
- uspto-grants-2010_09
- Patent number
- US07795283B2
Reaction notes
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