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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805259Generated: November 1, 2026

(3-Chlorophenyl)hydrazine → HCID 178419962, compound

https://huagongshe.com/reaction/1805259

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Chlorophenyl)hydrazineHCID 75332—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 3730890HCID 3730890—
SolventEthanolHCID 702—
ProductHCID 178419962HCID 178419962225.8%

Reaction Steps

To a solution of 0.5047 g (1.1994 mmol) methyl 3-(2-chloro-6-fluorophenyl)-5-(1-(dimethylamino)-4,4,4-trifluoro-3-oxobut-1-en-2-yl)isoxazole-4-carboxylate in dry ethanol, 0.1790 g (0.9995 mmol) 3-Chlorophenylhydrazine and 0.17 mL (0.9995 mmol) N,N-Diisopropylethylamine (DIPEA) were added. The reaction mixture was heated under reflux for 2 h. The product was isolated by using column chromatography (Petroleum ether:Diethyl ether 80:20), and 0.305 g (yield of theory: 61%) of the pyrazolyl-isoxazole derivative were obtained. Result of LC/MS [M+H]+: 499.9; 1H NMR (DMSO-d6; CCl4): 3.66 (3H, s, CH3), 7.45-7.50 (1H, dd, CH-arom.), 7.55-7.58 (1H, d, CH-arom.), 7.65-7.77 (1H, d, CH-arom.), 7.65-7.77 (1H, dd, CH-arom. phenylhydrazine), 7.65-7.77 (1H, d, CH-arom. phenylhydrazine), 7.85 (1H, s, CH-arom phenylhydrazine), 8.56 (1H, s, 1-pyrazole)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354436B2
Source datasetuspto-grants-2013_01
ORD IDord-ef8eb5c93d674f01a8aa54cf900f98ef
Source noteuspto-grants-2013_01