2,4-Dimethoxybenzoic acid → HCID 135522275, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:9]=[C:8]([O:10]C)[CH:7]=[CH:6][C:4]=1[NH2:5].C[O:13][C:14]1[CH:22]=[C:21]([O:23]C)[CH:20]=[CH:19][C:15]=1C(O)=O>>[OH:10][C:8]1[CH:7]=[CH:6][C:4]2[N:5]=[C:1]([C:20]3[CH:19]=[CH:15][C:14]([OH:13])=[CH:22][C:21]=3[OH:23])[O:2][C:3]=2[CH:9]=1Participants
3
Procedure
The title compound was prepared in substantially the same manner as described in Example 1, from 2,4-dimethoxyaniline, and 2,4-dimethoxybenzoic acid and was obtained as a white solid, m.p. 293–296° C.; MS m/e 242 (M−H)+.
Workup
- customwas obtained as a white solid, m.p. 293–296° C.
Sources & evidence
- ORD record
- ord-dd81ed602b3544bc84bb5be227e470d8
- Source dataset
- uspto-grants-2006_12
- Patent number
- US07148247B2
Reaction notes
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