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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853213Generated: October 29, 2026

Water → 7-Benzyloxy-6-cyano-4-(3-fluoro-4-nitrophenoxy)quinoline

https://huagongshe.com/reaction/853213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Fluoro-4-nitrophenolHCID 520948—
Reactant7-Benzyloxy-4-chloro-6-cyanoquinolineHCID 22646519—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product7-Benzyloxy-6-cyano-4-(3-fluoro-4-nitrophenoxy)quinolineHCID 2293664940%

Reaction Conditions

Temperature110 °C

Reaction Steps

The 7-benzyloxy-4-chloro-6-cyanoquinoline (8.82 g, 30.0 mmol) described in WO98/13350 was suspended in 1-methylpyrrolidone (30 ml), and then 3-fluoro-4-nitrophenol (5.18 g, 33.0 mmol) and N,N-diisopropylethylamine (3.88 g, 30.0 mmol) were added and the mixture was heated and stirred at 110° C. for 4 hours. After returning the reaction system to room temperature, water was added and a solid precipitated. The obtained solid was filtered out, washed with water, methanol and ethyl acetate and dried at 60° C. to obtain the title compound (4.98 g, 12.0 mmol, 40%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253286B2
Source datasetuspto-grants-2007_08
ORD IDord-40c2904126a74f718b043315e7309fda
Source noteuspto-grants-2007_08