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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111309Generated: November 2, 2026

N-(Phenylmethyl)-beta-alanine ethyl ester → 3-[Benzyl-(2-chloro-5-nitro-pyrimidin-4-yl)-amino]-propanoic acid ethyl ester

https://huagongshe.com/reaction/2111309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(Phenylmethyl)-beta-alanine ethyl esterHCID 90196—
ReactantPotassium BicarbonateHCID 516893—
Reactant2,4-Dichloro-5-nitropyrimidineHCID 521266—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product3-[Benzyl-(2-chloro-5-nitro-pyrimidin-4-yl)-amino]-propanoic acid ethyl esterHCID 5815413093.2%

Reaction Steps

A solution of 1.04 g (0.005 mole) of 3-benzylamino-propanoic acid ethyl ester in 20 mL of water was added dropwise to a solution of 0.97 g (0.005 mole) of 2,4-dichloro-5-nitro-pyrimidine in 20 mL of ethyl ether. At 0 degrees, 1.0 g (0.010 mole) of potassium bicarbonate was added. The mixture was stirred at ambient temperature for 3 hours. The layers were then separated, and the aqueous layer extracted twice with 30 mL of ether. The combined organic layers were dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. Purification by silica gel chromatography, eluting with hexanes-ethyl acetate (100:0-90:10) gave 1.70 g of 3-[benzyl-(2-chloro-5-nitro-pyrimidin-4-yl)-amino]-propanoic acid ethyl ester (IV-22).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517873B2
Source datasetuspto-grants-2009_04
ORD IDord-80e22fa1ad6a4cc39aac9fea4840ff29
Source noteuspto-grants-2009_04