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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926042Generated: November 1, 2026

3-Chloro-4-(3-fluorobenzyloxy)aniline → N-{3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}-1H-pyrazolo[4,3-d]pyrimidin-7-amine

https://huagongshe.com/reaction/1926042

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-4-(3-fluorobenzyloxy)anilineHCID 7059263—
ReactantPyridinium chlorideHCID 10176127—
Reactant7-(methylthio)-1H-pyrazolo[4,3-d]pyrimidineHCID 55295894—
SolventEthyl AcetateHCID 8857—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductN-{3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}-1H-pyrazolo[4,3-d]pyrimidin-7-amineHCID 5759722166%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 7-(methylthio)-1H-pyrazolo[4,3-d]pyrimidine (known compound from literature: J. Am. Chem. Soc., 1956, 78, 2418) (150 mg), 3-chloro-4-[(3-fluorobenzyl)oxy]aniline (227 mg) and pyridine hydrochloride (156 mg) in 1-methyl-2-pyrrolidone (3 mL) was stirred at 120° C. for 10 hrs. After the completion of the reaction, the mixture was diluted with ethyl acetate and washed with saturated aqueous sodium hydrogen carbonate and saturated brine. The organic layer was concentrated under reduced pressure, and the residue was subjected to silica gel column chromatography (hexane/ethyl acetate=1/3→1/10) to give the title compound (220 mg, yield 61%) as a pale-yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178543B2
Source datasetuspto-grants-2012_05
ORD IDord-83cb66cbe62e43e6931e15c7c12f4ff8
Source noteuspto-grants-2012_05