6-Methoxynicotinic acid → HCID 73425620, compound
Reaction equation
[NH2:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([CH3:14])([CH3:13])[C:7](=[O:12])[N:8]2[CH3:11])=[CH:4][CH:3]=1.[CH3:15][O:16][C:17]1[CH:25]=[CH:24][C:20]([C:21](O)=[O:22])=[CH:19][N:18]=1>>[CH3:15][O:16][C:17]1[CH:25]=[CH:24][C:20]([C:21]([NH:1][C:2]2[CH:10]=[C:9]3[C:5]([C:6]([CH3:14])([CH3:13])[C:7](=[O:12])[N:8]3[CH3:11])=[CH:4][CH:3]=2)=[O:22])=[CH:19][N:18]=1Participants
3
Procedure
Prepared in analogy to example 1b from 6-amino-1,3,3-trimethylindolin-2-one and 6-methoxynicotinic acid. The title compound was obtained as light yellow foam.
Sources & evidence
- ORD record
- ord-da62a43390f748b98d3bf24d2f6ee979
- Source dataset
- uspto-grants-2015_12
- Patent number
- US09221816B2
Reaction notes
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