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 lmL acetyl chloride, followed by addition of 2.0 g(17.84 mmol) of 4-pyrazolcarboxylic 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) δ8.25, 3.86.
Workup
- temperatureby warming the mixture
- temperatureat reflux for 18 h
- temperatureThe solution was cooled
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-872b31d9a7b542ba8f669274112e8122
- Source dataset
- uspto-grants-2000_09
- Patent number
- US06124334
Reaction notes
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