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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371453Generated: November 1, 2026

Benzoyl chloride → n-(1-Benzoylpiperidin-4-yl)-n'-{[4-(3,4-dichlorobenzyl)morpholin-2-yl]methyl}urea

https://huagongshe.com/reaction/1371453

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 17984664HCID 17984664—
SolventDichloromethaneHCID 6344—
Productn-(1-Benzoylpiperidin-4-yl)-n'-{[4-(3,4-dichlorobenzyl)morpholin-2-yl]methyl}ureaHCID 17984690—

Reaction Conditions

Temperature23 °C

Reaction Steps

Benzoyl choride (0.014 ml) was added to a solution of Intermediate 16 (0.04 g) and N,N-diisopropylethylamine (0.048 ml) in dichloromethane (3 ml). The solution was stirred for 5 h at 23° C. The solvent was removed in vacuo and the residue purified by solid phase extraction (Isolute SCX sulphonic acid column) eluting with methanol followed by 10% 0.880 ammonia solution in methanol. The basic fraction was concentrated in vacuo and the residue was further purified using a silica gel solid phase extraction cartridge (1 g Varian Bond Elut), eluting sequentially with dichloromethane, ethyl acetate, acetone, acetonitrile, and methanol, to give the title compound as a clear gum (0.024 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157457B2
Source datasetuspto-grants-2007_01
ORD IDord-ea26f59dc24c48f59bbc5afc970af945
Source noteuspto-grants-2007_01