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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926106Generated: November 3, 2026

3-Chloro-4-(3-fluorobenzyloxy)aniline → N-{3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}-5-(3-chloropropyl)-5H-pyrrolo[3,2-d]pyrimidin-4-amine

https://huagongshe.com/reaction/1926106

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-4-(3-fluorobenzyloxy)anilineHCID 7059263—
Reactant4-chloro-5-(3-chloropropyl)-5H-pyrrolo[3,2-d]pyrimidineHCID 86084830—
SolventIsopropanolHCID 3776—
ProductN-{3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}-5-(3-chloropropyl)-5H-pyrrolo[3,2-d]pyrimidin-4-amineHCID 6752063673.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 4-chloro-5-(3-chloropropyl)-5H-pyrrolo[3,2-d]pyrimidine (839 mg), 3-chloro-4-[(3-fluorobenzyl)oxy]aniline (1.10 g) and isopropyl alcohol (5 mL) was stirred at 80° C. for 1.5 hrs. The mixture was concentrated under reduced pressure, saturated aqueous sodium hydrogen carbonate (30 mL) was added to the residue, and the mixture was extracted with ethyl acetate (30 mL×3). The organic layers were combined, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent, hexane:ethyl acetate=90:10→20:80) to give the title compound (1.19 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178543B2
Source datasetuspto-grants-2012_05
ORD IDord-86845efe53ba4349ae506b03ed20db0c
Source noteuspto-grants-2012_05