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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298020Generated: October 30, 2026

1-Butanol → n-Butyl 3-methyl-1-(quinolin-5-yl)-1H-pyrazole-4-carboxylate

https://huagongshe.com/reaction/2298020

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-ButanolHCID 263—
ReactantHydrochloric AcidHCID 313—
ReactantSulfuric AcidHCID 1118—
Reactant5-AcetyluracilHCID 234581—
Reactant5-Hydrazinoquinoline dihydrochlorideHCID 12334107—
Productn-Butyl 3-methyl-1-(quinolin-5-yl)-1H-pyrazole-4-carboxylateHCID 2226779960%

Reaction Conditions

Temperature23 °C

Reaction Steps

A mixture of 5-acetyluracil (0.231 g, 1.5 mmol), 5-quinolinylhydrazine dihydrochloride (0.418 g, 1.8 mmol) and HCl (conc., 0.75 mL, 9 mmol) in n-butanol (15 mL) was heated at reflux for 20 h, cooled to 23° C., and concentrated in vacuo. The residue was dissolved in n-butanol (10 mL). The resulting solution was treated with H2SO4 (conc., 0.96 mL, 18 mmol), heated at reflux for 20 h, cooled to 23° C. and concentrated in vacuo. The residue was partitioned between EtOAc and NaOH (1 M). The aqueous layer was extracted three times with EtOAc. The combined organic extracts were dried over Na2SO4 and concentrated in vacuo. The brown solid residue was purified by flash chromatography (Flash 40S, hexanes-acetone 8:2) to afford 0.279 g (60%) of the desired product as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492401B1
Source datasetuspto-grants-2002_12
ORD IDord-5597ef102931449e9059a3b6d473b501
Source noteuspto-grants-2002_12