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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926164Generated: October 29, 2026

2-(2-(4-Chloro-5H-pyrrolo[3,2-d]pyrimidin-5-yl)ethoxy)ethyl benzoate → HCID 67521544, compound

https://huagongshe.com/reaction/1926164

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-(4-Chloro-5H-pyrrolo[3,2-d]pyrimidin-5-yl)ethoxy)ethyl benzoateHCID 56850803—
ReactantHCID 67520846HCID 67520846—
SolventIsopropanolHCID 3776—
ProductHCID 67521544HCID 6752154458%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2-[2-(4-chloro-5H-pyrrolo[3,2-d]pyrimidin-5-yl)ethoxy]ethyl benzoate (1.46 g), tert-butyl 4-(4-amino-2-chlorophenoxy)benzoate (1.35 g) and isopropyl alcohol (30 mL) was stirred at 80° C. overnight. The reaction mixture was concentrated under reduced pressure, water and saturated aqueous sodium hydrogen carbonate solution were added, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the obtained residue was subjected to silica gel column chromatography (eluent, ethyl acetate). The object fraction was concentrated under reduced pressure and the residue was crystallized from ethyl acetate-diethyl ether to give the title compound (1.54 g) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178543B2
Source datasetuspto-grants-2012_05
ORD IDord-15c7e17838aa4f80a5f853d72167335a
Source noteuspto-grants-2012_05