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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207365Generated: October 31, 2026

Sodium Carbonate → HCID 131735891, compound

https://huagongshe.com/reaction/2207365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant5-Bromo-2-fluoropyridineHCID 2783168—
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—
ProductHCID 131735891HCID 131735891—

Reaction Conditions

Temperature85 °C

Reaction Steps

2-Methyl-THF (123 mL), sodium carbonate (2M, 18.5 mL, 36.9 mmol) and 5-bromo-2-fluoropyridine (7.15 g, 40.6 mmol) were added to N-[3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-4-(trifluoromethyl)pyrimidin-2-amine (14 g, 36.9 mmol) and the reaction mixture was purged and flushed with Ar(g) (3×) before adding PdCl2(dppf)-dichloromethane adduct (1.51 g, 1.85 mmol). The reaction mixture was heated to 85° C. overnight. Another portion of 5-bromo-2-fluoropyridine (2.00 g) and PdCl2(dppf)-dichloromethane adduct (300 mg, 0.368 mmol) were added to the reaction mixture and heated to 85° C. overnight. The reaction mixture was cooled to room temperature and concentrated under reduced pressure. A hot solution of 10% water, 20% DCM and 70% MeCN was added to the residue and the product was collected by filtration. The product was washed with cold DCM to yield N-[3-(6-fluoropyridin-3-yl)-5-methylphenyl]-4-(trifluoromethyl)pyrimidin-2-amine as a green-tinted solid. MS APC calc'd for C17H13F3N4 [M+H]+ 349. found 349. 1H NMR (500 MHz, DMSO-d6) δ 10.27 (s, 1H), 8.82 (d, J=4.8 Hz, 1H), 8.45 (s, 1H), 8.18 (td, J=2.4 Hz, 8.2 Hz, 1H), 7.93 (s, 1H), 7.56 (s, 1H), 7.31-7.24 (m, 2H), 7.18 (s, 1H), 3.32 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376418B2
Source datasetuspto-grants-2016_06
ORD IDord-204b57084d574ae2baf184ac1769734a
Source noteuspto-grants-2016_06