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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387752Generated: October 28, 2026

Thioanisole → HCID 135829401, compound

https://huagongshe.com/reaction/387752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioanisoleHCID 7520—
ReactantHCID 22936427HCID 22936427—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 135829401HCID 13582940180%

Reaction Conditions

Temperature70 °C

Reaction Steps

The N-(4-(7-benzyloxy-6-cyanoquinolyl)oxy-2-fluorophenyl)-N′-(2-thiazolyl)urea (5.53 g) synthesized in Example 141 was dissolved in TFA (55 ml), and then thioanisole (5.5 ml) was added and the mixture was heated and stirred at 70° C. for 6 hours. After cooling the reaction solution and concentrating it under reduced pressure, bicarbonate water and methanol were added and the precipitated crystals were filtered. These were washed with diethyl ether to obtain 3.63 g of the title compound (80% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372981B2
Source datasetuspto-grants-2013_02
ORD IDord-552b09e598c34ed98db96afcf3941d44
Source noteuspto-grants-2013_02