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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715039Generated: October 29, 2026

Sodium Carbonate → N-(1-(3-(4-Cyanophenyl)-7-fluoro-4-oxo-4H-pyrido[1,2-a]pyrimidin-2-yl)ethyl)-N-(2-(ethylsulfonyl)ethyl)-2-(4-fluoro-3-(trifluoromethyl)phenyl)acetamide

https://huagongshe.com/reaction/1715039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Cyanophenylboronic acidHCID 2734326—
ReactantN-(1-(3-Bromo-7-fluoro-4-oxo-4H-pyrido[1,2-a]pyrimidin-2-yl)ethyl)-N-(2-(ethylsulfonyl)ethyl)-2-(4-fluoro-3-(trifluoromethyl)phenyl)acetamideHCID 58796903—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventTetrahydrofuranHCID 8028—
ProductN-(1-(3-(4-Cyanophenyl)-7-fluoro-4-oxo-4H-pyrido[1,2-a]pyrimidin-2-yl)ethyl)-N-(2-(ethylsulfonyl)ethyl)-2-(4-fluoro-3-(trifluoromethyl)phenyl)acetamideHCID 1604035754.6%

Reaction Steps

E5 (66.8 mg, 0.11 mmol), 4-cyanophenyl boronic acid (20 mg, 0.13 mmol), and Pd(dppf)2Cl2 (9 mg, 0.01 mmol) was added into a 10 mL CEM microwave tube, followed by THF (1.1 mL) and sodium carbonate (0.55 mL, 2M). The mixture was reacted by microwave at 150° C. for 10 min and then partitioned between water and ethyl acetate. Column chromatography with gradient dichloromethane:ethyl acetate (4:1 to 3:1 to 2:1) afforded 38 mg 7.01 as a yellow foamy solid in a racemic mixture. Additional amounts of 7.01 were prepared and combined.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799795B2
Source datasetuspto-grants-2010_09
ORD IDord-20e5da98d45d429ba00c1f45c9a72cd3
Source noteuspto-grants-2010_09