4-Methoxy-2-nitroaniline → HCID 9902590, compound
Reaction equation
[Cl:1][C:2]1[C:3]([Cl:11])=[N:4][CH:5]=[C:6]([CH:10]=1)[C:7]([OH:9])=O.[CH3:12][O:13][C:14]1[CH:20]=[CH:19][C:17]([NH2:18])=[C:16]([N+:21]([O-:23])=[O:22])[CH:15]=1>>[Cl:1][C:2]1[CH:10]=[C:6]([C:7]([NH:18][C:17]2[CH:19]=[CH:20][C:14]([O:13][CH3:12])=[CH:15][C:16]=2[N+:21]([O-:23])=[O:22])=[O:9])[CH:5]=[N:4][C:3]=1[Cl:11]Participants
3
Procedure
The title compound was prepared from 5,6-dichloronicotinic acid and 4-methoxy-2-nitroaniline and was obtained as a yellow solid as described in Example 15. 1H NMR (DMSO-d6): 10.85 (bs, 1H), 8.88 (d, J=2.4, 1H), 8.59 (d, J=2.4, 1H), 7.58-7.54 (m, 2H), 7.39-7.35 (m, 1H), 3.87 (s, 3H).
Workup
- customwas obtained as a yellow solid
Sources & evidence
- ORD record
- ord-c85bc233da514fa48c9c370f00883357
- Source dataset
- uspto-grants-2004_09
- Patent number
- US06794397B2
Reaction notes
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