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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672245Generated: October 26, 2026

Diethyl N-(4-aminobenzoyl)-L-glutamate → 2-[4-(Pyrimidin-2-ylamino)-benzoylamino]-pentanedioic acid diethyl ester

https://huagongshe.com/reaction/1672245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl N-(4-aminobenzoyl)-L-glutamateHCID 73002—
Reactant2-ChloropyrimidineHCID 74404—
SolventDimethylformamideHCID 6228—
Product2-[4-(Pyrimidin-2-ylamino)-benzoylamino]-pentanedioic acid diethyl esterHCID 6733420769.4%

Reaction Conditions

Temperature110 °C

Reaction Steps

2-Chloropyrimidine (0.72 g, 6.3 mmol) and N-(4-aminobenzoyl)-L-glutamic acid diethyl ester (2.04 g, 6.3 mmol, 1 equiv.) were dissolved in DMF (4 mL) and the resulting mixture was heated to 110° C. for 3 hrs. Reaction was complete as determined by TLC. The mixture was cooled to room temperature and partitioned between ethyl acetate and water. The organic phase was washed with brine, dried over MgSO4, and concentrated by rotavap. The residue was purified by column chromatography (silica gel, 50% EtOAc/hexane) to afford 1.75 g of desired product 2-[4-(pyrimidin-2-ylamino)-benzoylamino]-pentanedioic acid diethyl ester in 69% yield. MS (ESI) m/z 399.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998965B2
Source datasetuspto-grants-2011_08
ORD IDord-a3f651a449a84e309ce94b47b31d67f3
Source noteuspto-grants-2011_08