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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017437Generated: October 30, 2026

Diisopropylethylamine → Netupitant

https://huagongshe.com/reaction/1017437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
Reactant2-(3,5-Bis(trifluoromethyl)phenyl)-2-methylpropanoyl chlorideHCID 11267141—
Reactant3-Pyridinamine, N-methyl-4-(2-methylphenyl)-6-(4-methyl-1-piperazinyl)-HCID 15887412—
SolventDichloromethaneHCID 6344—
ProductNetupitantHCID 645114981%

Reaction Conditions

Temperature37.5 °C

Reaction Steps

A solution of 20 g (67.5 mmol) methyl-[6-(4-methyl-piperazin-1-yl)-4-o-tolyl-pyridin-3-yl]amine and 17.5 ml (101 mmol) N-ethyldiisopropylamine in 200 ml dichloromethane was cooled in an ice bath and a solution of 24 g (75 mmol) 2-(3,5-bis-trifluoromethyl-phenyl)-2-methyl-propionyl chloride in 50 ml dichloromethane was added dropwise. The reaction mixture was warmed to 35-40° C. for 3 h, cooled to room temperature again and was stirred with 250 ml saturated sodium bicarbonate solution. The organic layer was separated and the aqueous phase was extracted with dichloromethane. The combined organic layers were dried (magnesium sulfate) and evaporated. The residue was purified by flash chromatography to give 31.6 g (81%) of the title compound as white crystals. M.p. 155-157° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479483B2
Source datasetuspto-grants-2002_11
ORD IDord-239f61df2afa4900928c3518e41bd680
Source noteuspto-grants-2002_11