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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878393Generated: October 30, 2026

Triethylamine → Tert-butyl 4-(4-amino-3-fluorobenzoyl)-2,2-dimethylpiperazine-1-carboxylate

https://huagongshe.com/reaction/1878393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Amino-3-fluorobenzoic acidHCID 9971—
ReactantPropylphosphonic anhydrideHCID 111923—
Reactant1,1-Dimethylethyl 2,2-dimethyl-1-piperazinecarboxylateHCID 29922400—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 4-(4-amino-3-fluorobenzoyl)-2,2-dimethylpiperazine-1-carboxylateHCID 6687862283.3%

Reaction Steps

To tert-butyl 2,2-dimethylpiperazine-1-carboxylate (0.902 mmol, 0.193 g) in dichloro-methane (5 mL) was added 4-amino-3-fluorobenzoic acid (0.902 mmol, 0.14 g), and triethylamine (1.805 mmol, 0.252 mL, 0.183 g). To this mixture was added 1-propanephosphonic acid cyclic anhydride (1.805 mmol, 1.074 mL, 1.149 g, 50% solution in ethyl acetate). After 2 hours stirring, ethyl acetate was added and the organic mixture was washed with saturated sodium hydrogen carbonate, water, and saturated sodium chloride. The organic layer was dried with sodium sulfate, filtered and concentrated under vacuum to give the intermediate tert-butyl 4-(4-amino-3-fluorobenzoyl)-2,2-dimethylpiperazine-1-carboxylate (264 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314091B2
Source datasetuspto-grants-2012_11
ORD IDord-095b4c58d62f4a2d8bbe2ca1897e8abe
Source noteuspto-grants-2012_11