HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2350892Generated: October 27, 2026
Ethyl 2-chloroacetoacetate → 3-(Cyclopropylamino)-5-methyl-1H-pyrazole-4-carboxylic acid, ethyl ester hydrochloride
https://huagongshe.com/reaction/2350892
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 2-chloroacetoacetate | HCID 11858 | — |
| Reactant | 3-Amino-1-cyclopropylthiourea | HCID 1808158 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 3-(Cyclopropylamino)-5-methyl-1H-pyrazole-4-carboxylic acid, ethyl ester hydrochloride | HCID 14500713 | 30.9% |
Reaction Steps
A stirred slurry of 10.4 g (0.079 mole) of 4-cyclopropyl-3-thiosemicarbazide under nitrogen atmosphere was treated with 13 g (0.079 mole) of ethyl 2-chloroacetoacetate, stirred at ambient temperature for 1 hr, treated with 30 mL of 2N ethanolic hydrogen chloride and heated to reflux. The reaction mixture was allowed to cool to ambient temperature while stirring for ~72 hr. The sulfur residue was removed by filtration and the filtrate concentrated in vacuo to an orange oil which solidified. Recrystallization twice from acetone gave 7.4 g of large blade-like crystals, after drying for 2 hr at 98° C. under reduced pressure, mp 147°-148.5° C. The filtrates gave an additional 6 g of crude product. The 2 solids were combined ad recrystallized from methyl ethyl ketone to give 6.3 g of white crystalline power, mp 151°-152° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04871737 |
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| Source dataset | uspto-grants-1989_10 |
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| ORD ID | ord-be9ad077f6654d0c8da7bef8b41951ba |
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| Source note | uspto-grants-1989_10 |
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