Methanol → HCID 178498455, compound
Reaction equation
[C:1]([Cl:4])(=[O:3])C.[NH:5]1[CH:9]=[C:8](C(O)=O)[CH:7]=[N:6]1.[CH3:13][OH:14]>>[ClH:4].[NH:6]1[CH:7]=[CH:8][C:9]([C:13]([O:3][CH3:1])=[O:14])=[N:5]1Participants
4
Procedure
10 mL of methanol at 0° C. was treated dropwise with 1 mL acetyl chloride, followed by addition of 2.0 g (17.84 mmol) of 4-pyrazolecarboxylic acid, followed by warming the mixture at reflux for 18 h. The solution was cooled and concentrated in vacuo to afford 2.6 g (90%) of the title compound as a white solid. 1H NMR (CD3OD) δ 8.25, 3.86.
Workup
- temperatureby warming the mixture
- temperatureat reflux for 18 h
- temperatureThe solution was cooled
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-fddb126f6f9b43c8b0a4124cf41746df
- Source dataset
- uspto-grants-1999_06
- Patent number
- US05910504
Reaction notes
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