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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032122Generated: October 25, 2026

Tetrahydrofuran → 1-Propyl-4-[3-[3-(trifluoromethyl)phenoxy]-1-azetidinylcarbonyl]piperazine fumarate

https://huagongshe.com/reaction/1032122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantPotassium CarbonateHCID 11430—
ReactantN-Propylpiperazinium dibromideHCID 3085288—
Reactant1-Chlorocarbonyl-3-[3-(trifluoromethyl)phenoxy]azetidineHCID 19799606—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
Product1-Propyl-4-[3-[3-(trifluoromethyl)phenoxy]-1-azetidinylcarbonyl]piperazine fumarateHCID 1979959759.5%

Reaction Steps

A mixture of 2.8 g (0.01 mole) of 3-[3-(trifluoromethyl)phenoxy]-1-azetidinecarbonyl chloride and 4.2 g (0.03 mole) of potassium carbonate in 25 ml of tetrahydrofuran was stirred for 10 min, then treated with 2.9 g (0.01 mole) of 1-propylpiperazine dihydrobromide in small portions. After 30 min, a few pieces of ice were added. After stirring for 17 hr, the reaction was diluted with 200 ml of water then extracted with methylene chloride (2×50 ml). The combined extracts were dried over magnesium sulfate and concentrated in vacuo, yielding 4.84 g of crude residue. The residue was converted to the fumarate salt in 2-propanol, concentrated to a solid in vacuo and recrystallized from acetone with a trace of ethanol to yield 2.9 g (59.5%) of fine white crystals; m.p. 117°-123° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04956359
Source datasetuspto-grants-1990_09
ORD IDord-696ec00132224894a5fccc3f690cc770
Source noteuspto-grants-1990_09