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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750343Generated: October 27, 2026

Ethyl 4-chloroacetoacetate → ethyl 2-(2-(1-tert-butyl-5-(4-fluorophenyl)-1H-pyrazol-4-yl)thiazol-4-yl)acetate

https://huagongshe.com/reaction/1750343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-chloroacetoacetateHCID 69484—
Reactant1-tert-butyl-5-(4-fluorophenyl)-1H-pyrazole-4-carbothioamideHCID 86721180—
SolventEthanolHCID 702—
Productethyl 2-(2-(1-tert-butyl-5-(4-fluorophenyl)-1H-pyrazol-4-yl)thiazol-4-yl)acetateHCID 8672118198%

Reaction Steps

A solution of the compound (2.90 g, 10.46 mmol) obtained in step 4 and ethyl 4-chloroacetoacetate (1.554 mL, 11.50 mmol) in ethanol (30 mL) was stirred at 80° C. for 16 hr. The reaction mixture was concentrated under reduced pressure, and the residue was crystallized from ethyl acetate and hexane to give ethyl 2-(2-(1-tert-butyl-5-(4-fluorophenyl)-1H-pyrazol-4-yl)thiazol-4-yl)acetate (3.96 g, 10.22 mmol, 98%) as a pale-yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156837B2
Source datasetuspto-grants-2015_10
ORD IDord-ae005e53108e4cec84136c1075ee1ee3
Source noteuspto-grants-2015_10