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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172455Generated: October 27, 2026

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

https://huagongshe.com/reaction/1172455

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 numberUS07834018B2
Source datasetuspto-grants-2010_11
ORD IDord-3af61690d81549679bb88b34690dcf3c
Source noteuspto-grants-2010_11