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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515295Generated: October 30, 2026

Triethylamine → tert-Butyl 4-(4-(3-(2-amino-2-methylpropyl)ureido)-3-fluorobenzyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/515295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-MethylpropylenediamineHCID 13128—
Reactant4-Nitrophenyl chloroformateHCID 82129—
ReactantTert-butyl 4-(4-amino-3-fluorobenzyl)piperidine-1-carboxylateHCID 67193052—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 4-(4-(3-(2-amino-2-methylpropyl)ureido)-3-fluorobenzyl)piperidine-1-carboxylateHCID 8667094766%

Reaction Steps

tert-Butyl 4-(4-amino-3-fluorobenzyl)piperidine-1-carboxylate (3.44 mmol, 1.06 g) and 4-nitrophenyl chloroformate (3.44 mmol, 0.693 g) were combined in tetrahydrofuran (5 mL) and the reaction stirred at room temperature for 1 hour. 2-Methylpropane-1,2-diamine (3.44 mmol, 0.303 g) and triethylamine (10.31 mmol, 1.043 g) were added and the mixture stirred at room temperature overnight. The mixture was concentrated under reduced pressure and the resulting residue purified by silica gel column chromatography (eluting with dichloromethane to 20% methanol/dichloromethane) to afford the title compound (960 mg). MS (ESI) m/z 423.2 [M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108939B2
Source datasetuspto-grants-2015_08
ORD IDord-46e7ad5f7586464a8fef1c688ae03645
Source noteuspto-grants-2015_08