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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187764Generated: November 1, 2026

Potassium Carbonate → HCID 67501824, compound

https://huagongshe.com/reaction/1187764

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-5-(trifluoromethyl)pyridineHCID 92342—
ReactantHCID 66705807HCID 66705807—
SolventTolueneHCID 1140—
ProductHCID 67501824HCID 6750182438%

Reaction Conditions

Temperature110 °C

Reaction Steps

In a pressure tube, (S)-4-[2-(4-amino-phenyl)-ethyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (100 mg), 2-chloro-5-(trifluoromethyl)pyridine (57 mg) and potassium carbonate (431 mg) were combined with toluene (1 ml) to give a yellow solution. The mixture was degassed by bubbling through argon for several minutes. BINAP (12 mg) and palladium(II)acetate (2 mg) were then added and the tube was sealed. The reaction mixture was stirred at 110° C. for 1 hour. The reaction mixture was then cooled to room temperature and concentrated in vacuo. The residue was purified by flash chromatography (SiO2; gradient: 0% to 40% EtOAc in hexane) to afford (S)-2,2-dimethyl-4-{2-[4-(5-trifluoromethyl-pyridin-2-ylamino)-phenyl]-ethyl}-oxazolidine-3-carboxylic acid tert-butyl ester (55 mg, 38%) as a yellow amorphous solid. MS (ISP): 466.3 ([M+H]+), 410.2 ([M+H—C4H8]+), 366.2 ([M+H—C4H8—CO2]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673950B2
Source datasetuspto-grants-2014_03
ORD IDord-f3965a339bfd4d24b6e5504bfa7d510b
Source noteuspto-grants-2014_03