3-(2,2-Dimethyl-6-oxo-6H-[1,3]dioxin-4-yl)-benzonitrile → 3-(3-Cyano-phenyl)-N-[5-(3-methoxymethyl-pyrrol-1-yl)-2-nitro-phenyl]-3-oxo-propionamide
Reaction equation
[CH3:1][O:2][CH2:3][C:4]1[CH:8]=[CH:7][N:6]([C:9]2[CH:10]=[CH:11][C:12]([N+:16]([O-:18])=[O:17])=[C:13]([NH2:15])[CH:14]=2)[CH:5]=1.CC1(C)[O:25][C:24]([C:26]2[CH:27]=[C:28]([CH:31]=[CH:32][CH:33]=2)[C:29]#[N:30])=[CH:23][C:22](=O)[O:21]1>>[C:29]([C:28]1[CH:27]=[C:26]([C:24](=[O:25])[CH2:23][C:22]([NH:15][C:13]2[CH:14]=[C:9]([N:6]3[CH:7]=[CH:8][C:4]([CH2:3][O:2][CH3:1])=[CH:5]3)[CH:10]=[CH:11][C:12]=2[N+:16]([O-:18])=[O:17])=[O:21])[CH:33]=[CH:32][CH:31]=1)#[N:30]Participants
3
Procedure
The title compound was prepared from 5-(3-methoxymethyl-pyrrol-1-yl)-2-nitro-phenylamine (Example F7) and 3-(2,2-dimethyl-6-oxo-6H-[1,3]dioxin-4-yl)-benzonitrile (Example L1) according to the general procedure M. Obtained as a yellow solid (102 mg).
Sources & evidence
- ORD record
- ord-3df8bb3e3c5744afbfe1da60cddb5e06
- Source dataset
- uspto-grants-2003_04
- Patent number
- US06548495B2
Reaction notes
Loading…