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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407894Generated: October 27, 2026

Triethylamine → Tert-butyl 4-(2,5-dibromopentanamido)piperidine-1-carboxylate

https://huagongshe.com/reaction/407894

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
Reactant2,5-dibromopentanoyl BromideHCID 11163082—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-(2,5-dibromopentanamido)piperidine-1-carboxylateHCID 6746989290.5%

Reaction Steps

To a solution of crude 2,5-dibromopentanoyl bromide (6.50 g, 20 mmol) and triethylamine (3.06 g, 30.2 mmol) in CH2Cl2 (40 mL) cooled to 0° C. was added tert-butyl-4-aminopiperidine-1-carboxylate (4.23 g, 21.1 mmol) in one portion. The reaction was allowed to stir for 4 hours at which point the reaction was quenched by the addition of saturated aqueous NaHCO3 (5 mL) and CH2Cl2 (10 mL). The organic layer was separated and the aqueous layer washed with additional CH2Cl2 (3×15 mL). The combined organic layers were dried with MgSO4 and concentrated. The crude material was purified over silica gel (3:1 hexanes/EtOAc) to give tert-butyl 4-(2,5-dibromopentanamido)piperidine-1-carboxylate (8.00 g, 90%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754226B2
Source datasetuspto-grants-2014_06
ORD IDord-4f4be41b91b94cc4b110d48bc0d9419c
Source noteuspto-grants-2014_06