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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207393Generated: November 2, 2026

Sodium Carbonate → HCID 131735904, compound

https://huagongshe.com/reaction/2207393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant3-Bromo-5-fluoropyridineHCID 820206—
ReactantN-(3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-4-(trifluoromethyl)pyrimidin-2-amineHCID 58456089—
CatalystHCID 178418807HCID 178418807—
Solvent2-MethyltetrahydrofuranHCID 7301—
ProductHCID 131735904HCID 131735904—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of N-[3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-4-(trifluoromethyl)pyrimidin-2-amine (1.00 g, 2.64 mmol), Na2CO3 (2.64 mL, 5.27 mmol, 2.0 M), and 3-bromo-5-fluoropyridine (0.511 g, 2.90 mmol) in 2-methyl tetrahydrofuran (13.0 mL) was purged with argon (3×), then Pd(dppf)Cl2—CH2Cl2 (0.108 g, 0.132 mmol) was added. The reaction was purged with argon (3×) and heated to 80° C. The reaction was monitored by LC/MS and upon completion was cooled to ambient temperature. The reaction mixture was filtered through a CELITE plug and washed with dichloromethane. The eluent was diluted with water and the organic layer was extracted, dried over sodium sulfate, and concentrated in vacuo. The residue was purified by silica gel chromatography (acetone/hexanes) to afford N-[3-(5-fluoropyridin-3-yl)-5-methylphenyl]-4-(trifluoromethyl)pyrimidin-2-amine. MS APCI calc'd for C17H19F4N4 [M+H]+ 349. found 349.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376418B2
Source datasetuspto-grants-2016_06
ORD IDord-d30b530cd6994af09b89c714f4a7affb
Source noteuspto-grants-2016_06