2-Methyl-2H-pyrazol-3-ylamine → HCID 9922879, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([C:15]([OH:17])=O)=[C:7]2[C:11]=1[O:10][C:9]([CH2:12][O:13][CH3:14])=[CH:8]2.[CH3:18][N:19]1[C:23]([NH2:24])=[CH:22][CH:21]=[N:20]1>>[CH3:18][N:19]1[C:23]([NH:24][C:15]([C:6]2[CH:5]=[CH:4][C:3]([O:2][CH3:1])=[C:11]3[O:10][C:9]([CH2:12][O:13][CH3:14])=[CH:8][C:7]=23)=[O:17])=[CH:22][CH:21]=[N:20]1Participants
3
Procedure
Starting from 7-methoxy-2-methoxymethylbenzofuran-4-carboxylic acid (93 mg) and 2-methyl-2H-pyrazol-3-ylamine (40 mg). Purification by column chromatography on silica eluting with ethyl acetate afforded the title compound as a white solid (43 mg).
Workup
- customPurification by column chromatography on silica eluting with ethyl acetate
Sources & evidence
- ORD record
- ord-95c3de92d30d4112bb2afc4b513bb220
- Source dataset
- uspto-grants-2001_12
- Patent number
- US06331556B2
Reaction notes
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