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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867561Generated: November 3, 2026

Triethylamine → tert-Butyl 2-[[5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazol-3-yl]carbonyl]hydrazinecarboxylate

https://huagongshe.com/reaction/1867561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl carbazateHCID 70091—
Reactant5-(4-Chlorophenyl)-1-(2,4-dichlorophenyl)-4-methylpyrazole-3-carbonyl chlorideHCID 15284139—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 2-[[5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazol-3-yl]carbonyl]hydrazinecarboxylateHCID 8661835095.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 1.82 g of tert-butyl hydrazinecarboxylate and 2.4 ml of triethylamine in 50 ml of DCM is cooled to 0° C., a solution of 5.24 g of the compound obtained in stage A in 50 ml of DCM is added and the mixture is left stirring while allowing the temperature to rise to AT. The reaction mixture is washed with water, with a buffer solution at pH=2 and with a saturated NaHCO3 solution, the organic phase is dried over MgSO4 and the solvent is evaporated under vacuum. The residue is taken up in isopropyl ether, pentane is added and the precipitate formed is filtered off. 6.2 g of the expected compound are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632852B2
Source datasetuspto-grants-2009_12
ORD IDord-9f968290a2174829ac2a4e5b603a43a6
Source noteuspto-grants-2009_12