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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1894302Generated: November 1, 2026

Phosphorus oxychloride → 7-(Benzyloxy)-4-chloro-6-methoxyquinoline

https://huagongshe.com/reaction/1894302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 178486758HCID 178486758—
Product7-(Benzyloxy)-4-chloro-6-methoxyquinolineHCID 22646562—

Reaction Steps

7-Benzyloxy-6-methoxy-quinolin-4-ol (WO2006108059) (1 g) was refluxed with POCl3 (8 ml) for 3 hours. The reaction was evaporated and dissolved into DCM (80 ml) that was washed with ice water followed by brine. The organic layer was dried with Na2SO4 and evaporated to dryness to give a dark yellow solid as 4-chloro-7-benzyloxy-6-methoxy-quinoline that was mixed with 6-Hydroxy-N-methyl-1-naphthamide (600 mg), DMAP (1.5 eq) in dioxane (40 ml). The reaction was refluxed for three days and diluted with EtOAc, water and extracted with EtOAc three times. The combined organic layer was washed with water, brine and dried. The solution was evaporated and purified with silica gel column to give 6-(7-(benzyloxy)-6-methoxyquinolin-4-yloxy)-N-methyl-1-naphthamide (210 mg). This product was mixed with Pd/C (120 mg, 10%), HCONH4 (210 mg) in EtOH (20 ml). The mixture was refluxed for 1 hour and evaporated then mixed with water (2 ml). The solid was filtered and washed with water twice and cold MeOH as 6-(7-hydroxy-6-methoxyquinolin-4-yloxy)-N-methyl-1-naphthamide for next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513283B2
Source datasetuspto-grants-2013_08
ORD IDord-a085f707daf04767bc168537daaed222
Source noteuspto-grants-2013_08