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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2422152Generated: October 30, 2026

4-Chlorobenzoic Acid → HCID 59514566, compound

https://huagongshe.com/reaction/2422152

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzoic AcidHCID 6318—
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 59514507HCID 59514507—
SolventEthyl AcetateHCID 8857—
ProductHCID 59514566HCID 59514566—

Reaction Steps

A solution of methyl {4-chloro-6-(dimethylamino)-2-[4-(methylamino)benzyl]pyrimidin-5-yl}acetate (0.080 g, 0.23 mmol), 1-hydroxybenzotriazole (0.043 g, 0.32 mmol), triethylamine (0.11 mL, 0.80 mmol), and 4-chlorobenzoic acid (0.043 g, 0.28 mmol) was treated with WSCI (0.066 g, 0.34 mmol) at room temperature and the reaction mixture was stirred at room temperature for 16 hours. EtOAc was then added and the organic layer was washed sequentially with 0.5N HCl, saturated NaHCO3, and brine, dried over anhydrous Na2SO4, filtered, and concentrated to dryness to give the crude product methyl[4-chloro-2-{4-[(4-chlorobenzoyl)(methyl)amino]benzyl}-6-(dimethylamino)pyrimidin-5-yl]acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960393B2
Source datasetuspto-grants-2011_06
ORD IDord-87638c72fb6d4d24a43fe21e6c38926e
Source noteuspto-grants-2011_06