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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387179Generated: October 31, 2026

Methyl Acrylate → Methyl (2E)-3-(3-fluoro-2-((((2-methoxy-5-(trifluoromethyl)phenyl)amino)carbonyl)amino)phenyl)-2-propenoate

https://huagongshe.com/reaction/387179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl AcrylateHCID 7294—
Reactant4-QuinazolineAcetic Acid 8-Fluoro-1,2,3,4-Tetrahydro-3-[2-Methoxy-5-(TrifluoroMethyl)Phenyl]-2-Oxo-Methyl esterHCID 12001993—
ReactantN-(2-fluorophenyl)-N'-[2-methoxy-5-(trifluoromethyl)phenyl]ureaHCID 57857532—
ProductMethyl (2E)-3-(3-fluoro-2-((((2-methoxy-5-(trifluoromethyl)phenyl)amino)carbonyl)amino)phenyl)-2-propenoateHCID 57857531—

Reaction Steps

In addition, it has surprisingly been found that the structural unit methyl {8-fluoro-3-[2-methoxy-5-(trifluoromethyl)phenyl]-2-oxo-1,2,3,4-tetrahydroquinazolin-4-yl}acetate can be synthesized efficiently by means of an ortho-palladization. Here, N-(2-fluorophenyl)-N′-[2-methoxy-5-(trifluoromethyl)phenyl]urea is reacted with methyl acrylate and an oxidizing agent in the presence of an acid to give methyl (2E)-3-{3-fluoro-2-[({[2-methoxy-5-(trifluoromethyl)phenyl]amino}-carbonyl)amino]phenyl}acrylate. The ring closure to the tetrahydroquinazoline then follows under basic reaction conditions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372972B2
Source datasetuspto-grants-2013_02
ORD IDord-bcbb4a8948ed45e8890ce98ec3f715fe
Source noteuspto-grants-2013_02