Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448812Generated: October 25, 2026

Ethyl Acetate → 3-bromo-N-(4-chloro-2-(1-cyclopropylethylcarbamoyl)phenyl)-1-(3-chloropyridin-2-yl)-4,5-dihydro-1H-pyrazole-5-carboxamide

https://huagongshe.com/reaction/448812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
ReactantAcetic Acid Mixture with Hydrobromic AcidHCID 21893785—
Reactant5-(4-chloro-2-(1-cyclopropylethylcarbamoyl)phenylcarbamoyl)-1-(3-chloropyridin-2-yl)-4,5-dihydro-1H-pyrazol-3-yl2-nitrobenzene sulfonateHCID 86761927—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product3-bromo-N-(4-chloro-2-(1-cyclopropylethylcarbamoyl)phenyl)-1-(3-chloropyridin-2-yl)-4,5-dihydro-1H-pyrazole-5-carboxamideHCID 44185606—

Reaction Steps

400 mg of 5-(4-chloro-2-(1-cyclopropylethylcarbamoyl)phenylcarbamoyl)-1-(3-chloropyridin-2-yl)-4,5-dihydro-1H-pyrazol-3-yl2-nitrobenzene sulfonate was dissolved in 0.7 mL of acetic acid, and 0.3 mL of a 33 mass % hydrogen bromide acetic acid solution was dropwise added, followed by stirring for about one hour. After completion of the reaction, ethyl acetate, water and 2 mL of 1 N sodium hydroxide were added, followed by stirring and extraction with ethyl acetate. Then, concentration under reduced pressure was carried out to obtain a crude product. The crude product was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=3/2) to obtain 310 mg of the desired product in a paste form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481744B2
Source datasetuspto-grants-2013_07
ORD IDord-037c6414513d47b3a48280ee7fce0dc9
Source noteuspto-grants-2013_07