(4-Methoxy-2-nitro-phenyl)-carbamic acid tert-butyl ester → tert-butyl N-(2-amino-4-methoxyphenyl)carbamate
Reaction equation
[C:1]([O:5][C:6](=[O:19])[NH:7][C:8]1[CH:13]=[CH:12][C:11]([O:14][CH3:15])=[CH:10][C:9]=1[N+:16]([O-])=O)([CH3:4])([CH3:3])[CH3:2]>[Pd]>[C:1]([O:5][C:6](=[O:19])[NH:7][C:8]1[CH:13]=[CH:12][C:11]([O:14][CH3:15])=[CH:10][C:9]=1[NH2:16])([CH3:4])([CH3:2])[CH3:3]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound was prepared from (4-methoxy-2-nitro-phenyl)-carbamic acid tert-butyl ester (Example A10) by hydrogenation with 10% Pd/C according to the general procedure J (method a). Obtained as a white solid (19.377 g).
Sources & evidence
- ORD record
- ord-ee5cf85b8e56467cbb1d1bdafadded88
- Source dataset
- uspto-grants-2005_09
- Patent number
- US06949542B2
Reaction notes
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