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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butylhydrazine monohydrochlorideHCID 81889—
ReactantSodium AcetateHCID 517045—
Reactant2-(5-Chloroisoxazole-3-carbonyl)-3-dimethylamino-acrylic acid ethyl esterHCID 67021056—
SolventEthanolHCID 702—
Product1-tert-butyl-5-(5-chloro-isoxazol-3-yl)-1H-pyrazole-4-carboxylic acid ethyl esterHCID 6702104120,960.6%

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728029B2
Source datasetuspto-grants-2010_06
ORD IDord-1522ee36be9f4690889f8a1d7d6ebe25
Source noteuspto-grants-2010_06