Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159664Generated: October 29, 2026

4-Chlorobenzoic Acid → HCID 59514566, compound

https://huagongshe.com/reaction/1159664

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-chloro-benzoyl)(methyl)amino]benzyl}-6-(dimethylamino)pyrimidin-5-yl]acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812160B2
Source datasetuspto-grants-2010_10
ORD IDord-8903b1a602d14fad8832d148b3ecd712
Source noteuspto-grants-2010_10