HCID 69779703, compound → HCID 69779823, compound
Reaction equation
[C:1]([O:5][C:6](=[O:27])[NH:7][C:8]1[CH:13]=[C:12]([O:14][CH2:15][CH2:16][O:17][CH3:18])[C:11]([N:19]2[CH:23]=[CH:22][CH:21]=[CH:20]2)=[CH:10][C:9]=1[N+:24]([O-])=O)([CH3:4])([CH3:3])[CH3:2]>[Ni]>[C:1]([O:5][C:6](=[O:27])[NH:7][C:8]1[CH:13]=[C:12]([O:14][CH2:15][CH2:16][O:17][CH3:18])[C:11]([N:19]2[CH:23]=[CH:22][CH:21]=[CH:20]2)=[CH:10][C:9]=1[NH2:24])([CH3:4])([CH3:2])[CH3:3]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound was prepared from [5-(2-methoxy-ethoxy)-2-nitro-4-pyrrol-1-yl-phenyl]-carbamic acid tert.-butyl ester (Example A3) by hydrogenation with Raney-Nickel according to the general procedure J (method a). Obtained as an orange solid (196 mg).
Sources & evidence
- ORD record
- ord-d7699b2c201541cda72408e0b12b5f5b
- Source dataset
- uspto-grants-2003_04
- Patent number
- US06548495B2
Reaction notes
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