HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12876Generated: October 25, 2026
tert-Butylhydrazine monohydrochloride → 1-tert-butyl-5-(5-chloro-isoxazol-3-yl)-1H-pyrazole-4-carboxylic acid ethyl ester
https://huagongshe.com/reaction/12876
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butylhydrazine monohydrochloride | HCID 81889 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 2-(5-Chloroisoxazole-3-carbonyl)-3-dimethylamino-acrylic acid ethyl ester | HCID 67021056 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-tert-butyl-5-(5-chloro-isoxazol-3-yl)-1H-pyrazole-4-carboxylic acid ethyl ester | HCID 67021041 | 20,960.6% |
Reaction Steps
A solution of 2-(5-chloro-isoxazole-3-carbonyl)-3-dimethylamino-acrylic acid ethyl ester (294.8 mg, 1.08 mmol) in absolute ethanol (1.4 mL, 0.77M) was treated with tert-butylhydrazine hydrochloride (137.3 mg, 1.10 mmol) and sodium acetate (108.6 mg, 1.32 mmol). The resulting mixture was heated to 90° C. overnight. At this time, the reaction was cooled to 25° C. and was concentrated in vacuo. The reaction was partitioned between water (200 mL) and dichloromethane (2×50 mL). The combined organics were washed with a saturated aqueous sodium chloride solution, dried over magnesium sulfate, filtered and concentrated in vacuo. Biotage chromatography (40S column 60% ethyl acetate/hexanes) followed by ISCO CombiFlash (4 g column 0-20% ethyl acetate/hexanes) afforded 1-tert-butyl-5-(5-chloro-isoxazol-3-yl)-1H-pyrazole-4-carboxylic acid ethyl ester (67.4 g, 21%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07728029B2 |
|---|
| Source dataset | uspto-grants-2010_06 |
|---|
| ORD ID | ord-1522ee36be9f4690889f8a1d7d6ebe25 |
|---|
| Source note | uspto-grants-2010_06 |
|---|