2-Chlorobenzaldehyde → (2-Amino-4-chloro-5-methoxyphenyl)(2-chlorophenyl)-methanone
Reaction equation
[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]=[O:5].[Cl:10][C:11]1[CH:12]=[C:13]([CH:15]=[CH:16][C:17]=1[O:18][CH3:19])[NH2:14]>>[NH2:14][C:13]1[CH:12]=[C:11]([Cl:10])[C:17]([O:18][CH3:19])=[CH:16][C:15]=1[C:4]([C:3]1[CH:6]=[CH:7][CH:8]=[CH:9][C:2]=1[Cl:1])=[O:5]Participants
3
Procedure
(2-amino-4-chloro-5-methoxyphenyl)-(2-chlorophenyl)-methanone (Xy) was prepared by reacting 2-chlorobenzaldehyde with 0.019 moles of 3-chloro-4-methoxy aniline in a manner analogous to Example 1. MH+/Z=296.
Sources & evidence
- ORD record
- ord-e4b601179dd7457ca06002ce87bff4c5
- Source dataset
- uspto-grants-2009_04
- Patent number
- US07524840B2
Reaction notes
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