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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725511Generated: November 1, 2026

Potassium Phosphate, Tribasic → Tert-butyl 4-(3-cyclopropyl-2-fluorobenzoyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1725511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTricyclohexylphosphineHCID 75806—
ReactantCyclopropylboronic acidHCID 2760897—
ReactantTert-butyl 4-(3-bromo-2-fluorobenzoyl)piperazine-1-carboxylateHCID 57562603—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductTert-butyl 4-(3-cyclopropyl-2-fluorobenzoyl)piperazine-1-carboxylateHCID 57562614—

Reaction Conditions

Temperature150 °C

Reaction Steps

To a solution of 107 mg of tert-butyl 4-(3-bromo-2-fluorobenzoyl)piperazine-1-carboxylate in 2.0 ml of toluene and 0.1 ml of water was added 72 mg of cyclopropylboronic acid, 3.2 mg of palladium acetate, 0.052 ml of tricyclohexylphosphine (15% toluene solution) and 207 mg of potassium phosphate, successively. The reaction solution was stirred at 150° C. for 10 minutes using a microwave reaction apparatus. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine and then concentrated. The residue was purified by a silica gel column chromatography (eluent: hexane to hexane/ethyl acetate=1/1) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491720B2
Source datasetuspto-grants-2009_02
ORD IDord-fc6016df2a674420a3ce9f64387adc37
Source noteuspto-grants-2009_02