Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839658Generated: October 25, 2026

Oxalyl chloride → 1-Piperidinepropanoyl chloride

https://huagongshe.com/reaction/1839658

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant1-Piperidinepropanoic acidHCID 117782—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product1-Piperidinepropanoyl chlorideHCID 22561913—

Reaction Steps

To a solution of 3-piperidin-1-yl-propionic acid (472 mg, 3 mmol) in DCM (15 mL) at 0° C. was added oxalyl chloride (4.5 mmol) followed by one drop of DMF. After stirring for 2 hours at rt, the solvent was removed to give 3-piperidin-1-yl-propionyl chloride as a white solid. To a solution of 1,4,5,6,7,8-hexahydro-pyrrolo[3,2-b]azepine (347 mg, 2.55 mmol) in DCM (10 mL) was added TEA (1 eq.) and 1-piperidinepropionic acid chloride. The mixture was stirred at rt for overnight. The reaction was diluted with DCM, washed with NaHCO3, brine, dried and concentrated. The residue was purified on a silica gel column to give 230 mg of 3-piperidin-1-yl-1-(5,6,7,8-tetrahydro-1H-pyrrolo[3,2-b]azepin-4-yl)-propan-1-one as a light brown gel.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677368B2
Source datasetuspto-grants-2004_01
ORD IDord-9cf9019cfc044e9d80a4a439f9b2e6a8
Source noteuspto-grants-2004_01