Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474773Generated: October 30, 2026

N-[2-(4-{[4-Chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)ethyl]-N-methylguanidine → HCID 178494133, compound

https://huagongshe.com/reaction/474773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[2-(4-{[4-Chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)ethyl]-N-methylguanidineHCID 67775141—
ReactantMethyl 2-formyl-3-(2-methoxypyrimidin-5-yl)propanoateHCID 86666188—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 178494133HCID 17849413318.6%

Reaction Conditions

Temperature200 °C

Reaction Steps

To the solution of N-[2-(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)ethyl]-N-methylguanidine (100 mg, 0.269 mmol), methyl 2-formyl-3-[2-(methyloxy)-5-pyrimidinyl]propanoate (78 mg, 0.350 mmol) in NMP (5 mL) was added neat N-[2-(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)ethyl]-N-methylguanidine (100 mg, 0.269 mmol). The reaction mixture was heated with a microwave reactor at 200° C. for 2 h. Purification via MDAP then afforded the title compound as a white solid (33 mg, 0.050 mmol, 18.5% yield). LCMS: rt=3.14 min, [M+H+]=545.9

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637536B2
Source datasetuspto-grants-2014_01
ORD IDord-9fa6703139134473b55b172d2aea4b36
Source noteuspto-grants-2014_01