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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010415Generated: October 31, 2026

Thioanisole → N-(2-chloro-4-(6-cyano-7-hydroxyquinolin-4-yloxy)phenyl)-N'-methylurea

https://huagongshe.com/reaction/1010415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioanisoleHCID 7520—
ReactantHCID 22936876HCID 22936876—
SolventTrifluoroacetic acidHCID 6422—
ProductN-(2-chloro-4-(6-cyano-7-hydroxyquinolin-4-yloxy)phenyl)-N'-methylureaHCID 135829408109.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

After adding N-[4-(7-benzyloxy-6-cyanoquinolin-4-yloxy)-2-chlorophenyl]-N′-methylurea (968 mg) and thioanisole (3.7 ml) to trifluoroacetic acid (10 ml), the mixture was stirred overnight at 50° C. It was then concentrated under reduced pressure, ethyl acetate and aqueous sodium bicarbonate were added and the precipitated crystals were filtered out and washed with ethyl acetate to obtain the title compound (849 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973160B2
Source datasetuspto-grants-2011_07
ORD IDord-e1b97c36b9c54e6b95e986853afc01ff
Source noteuspto-grants-2011_07