4-amino-3-methoxy-N-(1-methylpyrrolidin-3-yl)benzamide → HCID 68683424, compound
Reaction equation
NC1C=CC(C(NC2CCN(C)C2)=O)=CC=1OC.[CH3:19][O:20][C:21]1[CH:22]=[C:23]([CH:34]=[CH:35][C:36]=1[N+:37]([O-])=O)[C:24]([NH:26][CH2:27][CH2:28][N:29]1[CH2:33][CH2:32][CH2:31][CH2:30]1)=[O:25]>>[NH2:37][C:36]1[CH:35]=[CH:34][C:23]([C:24]([NH:26][CH2:27][CH2:28][N:29]2[CH2:33][CH2:32][CH2:31][CH2:30]2)=[O:25])=[CH:22][C:21]=1[O:20][CH3:19]Participants
3
Procedure
The title compound was prepared in quantitative yield by an analogous method to the preparation of Intermediate 187, on a 2 g scale utilising 3-methoxy-4-nitro-N-(2-pyrrolidin-1-ylethyl)benzamide (Intermediate 193).
Sources & evidence
- ORD record
- ord-9a6eb6f912124e238c5b484ace202ec0
- Source dataset
- uspto-grants-2010_05
- Patent number
- US07709471B2
Reaction notes
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