HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350124Generated: October 30, 2026
Dimethylformamide → HCID 23024988, compound
https://huagongshe.com/reaction/350124
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 23024741 | HCID 23024741 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 23024988 | HCID 23024988 | 94.1% |
Reaction Steps
A mixture of 3-isopropyl-1-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyl]-1H-pyrazol-4-carboxylic acid (10.09 g), iodomethane (2 ml), potassium carbonate (4.83 g) and N,N-dimethylformamide (50 ml) was stirred at 80° C. for 5 hours. The reaction mixture was poured into water, which was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride solution, dried (MgSO4), then concentrated. The residue was subjected to silica gel column chromatography, and methyl 3-isopropyl-1-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyl]-1H-pyrazol-4-carboxylate (9.80 g, yield: 94%) was obtained as colorless crystals from the fraction eluted with ethyl acetate-hexane (1:2, volume ratio). This was recrystallized from ethyl acetate-hexane. Melting point: 90–91° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07179823B1 |
|---|
| Source dataset | uspto-grants-2007_02 |
|---|
| ORD ID | ord-18e6121447e54b29af11448833cdbf32 |
|---|
| Source note | uspto-grants-2007_02 |
|---|