Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111289Generated: November 1, 2026

Potassium Bicarbonate → (Rac)-2-{[(2-chloro-5-nitro-pyrimidin-4-yl)-cyclopentyl-amino]-methyl}-butanoic acid ethyl ester

https://huagongshe.com/reaction/2111289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium BicarbonateHCID 516893—
Reactant2,4-Dichloro-5-nitropyrimidineHCID 521266—
Reactant(Rac)-2-cyclopentylaminomethyl-butanoic acid ethyl esterHCID 57635035—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product(Rac)-2-{[(2-chloro-5-nitro-pyrimidin-4-yl)-cyclopentyl-amino]-methyl}-butanoic acid ethyl esterHCID 8755610470.1%

Reaction Steps

A solution of 1.07 g (0.005 mole) of (rac)-2-cyclopentylaminomethyl-butanoic acid ethyl ester in 25 mL of water was added dropwise to a solution of 0.97 g (0.005 mole) of 2,4-dichloro-5-nitro-pyrimidine in 25 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 (100:0-80:20) gave 1.3 g of (rac)-2-{[(2-chloro-5-nitro-pyrimidin-4-yl)-cyclopentyl-amino]-methyl}-butanoic acid ethyl ester (IV-12).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517873B2
Source datasetuspto-grants-2009_04
ORD IDord-a52733be9a59473096e061149a86462a
Source noteuspto-grants-2009_04