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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433402Generated: October 30, 2026

Thioanisole → HCID 135829401, compound

https://huagongshe.com/reaction/1433402

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, sodium bicarnobate 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 numberUS07612092B2
Source datasetuspto-grants-2009_11
ORD IDord-71a2f0151c1d421fbe361f25e1adf316
Source noteuspto-grants-2009_11