Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109851Generated: November 1, 2026

Dimethylformamide → tert-Butyl 4-{3-[4-(4-fluorobenzyl)-3-oxopiperazin-1-yl]-3-oxopropyl}piperidine-1-carboxylate

https://huagongshe.com/reaction/2109851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantHOAtHCID 181649—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant2-[1-(Tert-butoxycarbonyl)piperidin-4-yl]propanoic acidHCID 17781891—
Reactant1-(4-Fluorobenzyl)piperazin-2-oneHCID 18538638—
Producttert-Butyl 4-{3-[4-(4-fluorobenzyl)-3-oxopiperazin-1-yl]-3-oxopropyl}piperidine-1-carboxylateHCID 57634639—

Reaction Steps

To a solution of 1-boc-piperidin-4-ylpropionic acid (1.20 g, 4.7 mmol, Astatech) in DMF (10 mL), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (1.16 g, 6.1 mmol) and 1-hydroxy-7-azabenzotriazole (0.83 g, 6.1 mmol) were added and the solution was stirred at room temperature for 30 min. To the resultant solution, a solution of 1-(4-fluorobenzyl)piperazin-2-one (1.07 g, 5.1 mmol, see Example 31, Steps 5-8) in DMF (2 mL) was added and the mixture was stirred for two hours. The product mixture was concentrated under vacuum, and the residue partitioned between water and ethyl acetate. The combined organic extracts were washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by flash column chromatography (ISCO column, 120 g silica gel) eluting with a 0-6% MeOH/CHCl3 gradient over 40 min. Collection and concentration of appropriate fractions provided the coupled product as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517532B2
Source datasetuspto-grants-2009_04
ORD IDord-ae165f3ae2584ab292a1bdd94fcc904e
Source noteuspto-grants-2009_04