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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408870Generated: October 26, 2026

Triethylamine → Tert-butyl 4-(4-amino-3-fluorobenzoyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/408870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Amino-3-fluorobenzoic acidHCID 9971—
ReactantPropylphosphonic anhydrideHCID 111923—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 4-(4-amino-3-fluorobenzoyl)piperazine-1-carboxylateHCID 5805581591.7%

Reaction Steps

To a stirred solution of 4-amino-3-fluorobenzoic acid (4.97 g, 32.04 mmol), tert-butyl piperazine-1-carboxylate (5.97 g, 32.04 mmol) and triethylamine (10 mL) in dichloromethane (100 mL) was added 1-propanephosphonic acid cyclic anhydride (20 mL, 50% solution in ethyl acetate, dropwise). The reaction mixture was stirred for 1 hour then was diluted with ethyl acetate, washed with potassium carbonate (aqueous), dried (magnesium sulfate) and concentrated under reduced pressure to give the title compound (9.5 g). MS (ESI) m/z: 324.5 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759352B2
Source datasetuspto-grants-2014_06
ORD IDord-64ce207decc04c1aa951166ab423390d
Source noteuspto-grants-2014_06