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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098315Generated: November 3, 2026

Chlorosuccinimide → 4-chloro-2,N-dimethyl-5-morpholin-4-ylbenzamide

https://huagongshe.com/reaction/1098315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
Reactant2,N-dimethyl-5-morpholin-4-ylbenzamideHCID 23156888—
SolventDimethylformamideHCID 6228—
Product4-chloro-2,N-dimethyl-5-morpholin-4-ylbenzamideHCID 2315680147.5%

Reaction Conditions

Temperature50 °C

Reaction Steps

100 mg (0.427 mmol) of 2,N-dimethyl-5-morpholin-4-ylbenzamide prepared in Step A was dissolved in 3 ml of N,N-dimethylformamide, and thereafter, 63 mg (0.47 mmol) of N-chlorosuccinimide was added thereto under cooling on ice. The obtained mixture was stirred at 50° C. for 1 hour. Thereafter, the reaction solution was concentrated, and water was then added thereto. The mixture was extracted with ethyl acetate. The extract was washed with water and a saturated saline solution, and was then dried over anhydrous sodium sulfate. The extract was concentrated, and the obtained residue was then purified by silica gel column chromatography (ethyl acetate:methylene chloride=1:5), so as to obtain 54.5 mg (47%) of 4-chloro-2,N-dimethyl-5-morpholin-4-ylbenzamide in the form of a colorless solid, as well as 46 mg (40%) of 2-chloro-6,N-dimethyl-3-morpholin-4-ylbenzamide in the form of a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143274B2
Source datasetuspto-grants-2012_03
ORD IDord-b97a92208f8d4307a7900e85a7f3f48b
Source noteuspto-grants-2012_03