HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570825Generated: October 31, 2026
Hydrochloric Acid → HCID 178469942, compound
https://huagongshe.com/reaction/570825
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 59580024 | HCID 59580024 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178469942 | HCID 178469942 | — |
Reaction Steps
A suspension of 1-acetyl-3-oxo-2,3-dihydro-1H-pyrazole-4-carboxilic acid ethyl ester (2.7 g, This compound was prepared in a similar manner to that described in Bioorganic & Medicinal Chemistry Letters (2002), 12 (16), 2105-2108), benzylbromide (2.5 g), potassium carbonate (2.1 g) in N,N-dimethylformamide (20 mL) was stirred at 40° C. for 20 hours. To this reaction mixture was added 1 mol/L hydrochloric acid, and this mixture was extracted with ethyl acetate. This organic layer was washed with brine, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure. The residue was purified by column chromatography on aminopropyl silica gel (eluent: ethyl acetate/n-hexane) to give the title compound (1.6 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09023882B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-475e135ec9c34086a49d5266217b29c3 |
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| Source note | uspto-grants-2015_05 |
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