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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217877Generated: October 29, 2026

8-(4-amino-3-fluorophenoxy)pyrido[2,3-b]pyrazin-3(4H)-one → 1-(2-Fluoro-4-(3-oxo-3,4-dihydropyrido[3,2-b]pyrazin-8-yloxy)phenyl)-3-(2-(pyridin-3-yloxy)-5-(trifluoromethyl)phenyl)urea

https://huagongshe.com/reaction/217877

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-(4-amino-3-fluorophenoxy)pyrido[2,3-b]pyrazin-3(4H)-oneHCID 46900932—
ReactantPhenyl 2-(pyridin-3-yloxy)-5-(trifluoromethyl)phenylcarbamateHCID 59588873—
Product1-(2-Fluoro-4-(3-oxo-3,4-dihydropyrido[3,2-b]pyrazin-8-yloxy)phenyl)-3-(2-(pyridin-3-yloxy)-5-(trifluoromethyl)phenyl)ureaHCID 44131882—

Reaction Steps

Method F2 was used with 8-(4-amino-3-fluorophenoxy)pyrido[2,3-b]pyrazin-3(4H)-one (30.6 mg, 0.112 mmol) and a 60.6 mM solution of phenyl 2-(pyridin-3-yloxy)-5-(trifluoromethyl)phenylcarbamate (1.6 ml, 0.097 mmol). After 40 h, the mixture was evaporated onto silica gel, loaded onto a Biotage 12+M column, which was eluted with 40%-100% EtOAc in DCM. Yield: 4 mg (7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198279B2
Source datasetuspto-grants-2012_06
ORD IDord-03d6fb8b116044cbb117e4f9692f95b2
Source noteuspto-grants-2012_06