1H-Pyrazol-3-amine, 5-methyl- → N-(5-methyl-1H-pyrazol-3-yl)acetamide
Reaction equation
[NH:1]1[CH:5]=[CH:4][C:3]([NH:6][C:7](=[O:9])[CH3:8])=[N:2]1.[CH3:10]C1NN=C(N)C=1>>[CH3:10][C:5]1[NH:1][N:2]=[C:3]([NH:6][C:7](=[O:9])[CH3:8])[CH:4]=1Participants
3
Procedure
Title compound was prepared by a method analogous to that described for Intermediate 1, replacing 1H-pyrazol-3-amine with 5-methyl-1H-pyrazol-3-amine. (ALDRICH, 1.01 g, 7.25 mmol, 70.4% yield). 1H NMR (300 MHz, DMSO-d6) δ ppm: 11.89 (s, 1H), 10.16 (s, 1H), 6.22 (s, 1H), 2.16 (s, 3H), 1.94 (s, 3H). [ES+MS] m/z 140 (MH+).
Sources & evidence
- ORD record
- ord-b38ae73a315c49558b1b1d17c0f995f8
- Source dataset
- uspto-grants-2016_05
- Patent number
- US09334265B2
Reaction notes
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