3-Chloro-4-methoxyaniline → 1-(2-Amino-4-chloro-5-methoxyphenyl)ethanone
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:6]=[CH:7][C:8]=1[O:9][CH3:10])[NH2:5].NC1C=[C:16]([O:18]C)[CH:15]=CC=1C(=O)C>>[NH2:5][C:4]1[CH:3]=[C:2]([Cl:1])[C:8]([O:9][CH3:10])=[CH:7][C:6]=1[C:16](=[O:18])[CH3:15]Participants
3
Procedure
40 g. Compound 40 g was synthesized from 3-chlor-4-methoxy-aniline 39 g as a brown solid in 50% yield, according to the procedure as described for compound 40a.
Sources & evidence
- ORD record
- ord-b5b839ec4ebc462fa5fc125f8348f9d4
- Source dataset
- uspto-grants-2011_08
- Patent number
- US08003659B2
Reaction notes
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