5-Fluoro-2-methoxyaniline → HCID 67320747, compound
Reaction equation
[Cl:1][C:2]1[CH:26]=[CH:25][C:24]([Cl:27])=[CH:23][C:3]=1[O:4][C:5]1[CH:10]=[CH:9][N:8]=[CH:7][C:6]=1[C:11](N1C2C(=CC=CC=2)CCC1)=[O:12].[F:28][C:29]1[CH:30]=[CH:31][C:32]([O:36][CH3:37])=[C:33]([NH2:35])[CH:34]=1>>[Cl:1][C:2]1[CH:26]=[CH:25][C:24]([Cl:27])=[CH:23][C:3]=1[O:4][C:5]1[C:6]([C:11]([NH:35][C:33]2[CH:34]=[C:29]([F:28])[CH:30]=[CH:31][C:32]=2[O:36][CH3:37])=[O:12])=[CH:7][N:8]=[CH:9][CH:10]=1Participants
3
Procedure
The title compound was prepared in analogy to Example 1, from 4-(2,5-dichloro-phenoxy)-nicotinic acid (Example 1, intermediate) and 5-fluoro-2-methoxy-phenylamine (commercially available; CAS RN 1978-39-8). White solid (74%). MS (ESI): m/z=407.036 [M+H]+.
Sources & evidence
- ORD record
- ord-dae61c5fc8eb4b00b03631673126c294
- Source dataset
- uspto-grants-2014_05
- Patent number
- US08729091B2
Reaction notes
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