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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846676Generated: November 2, 2026

Chloroacetic Acid → HCID 67322178, compound

https://huagongshe.com/reaction/1846676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetic AcidHCID 300—
ReactantHCID 67323078HCID 67323078—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 67322178HCID 6732217811%

Reaction Steps

A mixture of 0.100 g (0.285 mmol) of 3-chloro-N-(5-chloro-2-piperazin-1-yl-pyridin-3-yl)-benzamide and 0.040 g (0.43 mmol) of chloroacetic acid in N,N-dimethylformamide is stirred overnight at room temperature then heated to 100° C. for 24 hours. The mixture is cooled to room temperature, diluted with water, and extracted with ethyl acetate. The aqueous phase is concentrated under reduced pressure and the residue is purified by preparative reverse phase HPLC to provide 0.009 g (11%) of {4-[5-chloro-3-(3-chloro-benzoylamino)-pyridin-2-yl]-piperazin-1-yl}-acetic acid as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952004B2
Source datasetuspto-grants-2015_02
ORD IDord-c4979ca620fc499f80226eb886c97c4e
Source noteuspto-grants-2015_02