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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481305Generated: October 31, 2026

Potassium Carbonate → HCID 19066087, compound

https://huagongshe.com/reaction/481305

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-5-(trifluoromethyl)pyridineHCID 92342—
ReactantHCID 178470820HCID 178470820—
SolventAcetoneHCID 180—
ProductHCID 19066087HCID 1906608757%

Reaction Conditions

Temperature65 °C

Reaction Steps

2-Chloro-5-trifluoromethylpyridine (Ishihara Corporation, 600 Montgomery St., San Francisco, Calif. 94111) (0.5 g, 2.8 mmol) and 5-(2-ethoxy-2-oxoethyl)-2-mercapto-4-methyl-1,3-thiazole (K. Fleishmann, K. H. Scheunemann, H. U. Schortemmer, G. Dickneite, J. Blumbad, G. F. Fischer, W. Durckheimer, and H. H. Sedlacek, Arzneim-Forsch./Drug Res., 1989, 39(II), 743) (0.6 g, 2.8 mmol) were dissolved in acetone (15 ml) under a reaction inert atmosphere. Freshly ground K2CO3 (0.42 g, 3.0 mmol) was added to this solution and the reaction was heated to 65° C. for 16 hours. The K2CO3 was filtered off and the acetone was removed via rotary evaporation. The remaining slurry was diluted with a saturated aqueous solution of sodium bicarbonate, extracted three times (200 ml) with methylene chloride, dried over MgSO4 and filtered. The solvent was then stripped off and the resulting solid was purified via flash chromatography (50% ether in hexane) to afford the title compound of this Example (0.57 g, 57% yield). 1H NMR (CDCl3): δ 8.69 (1H, d, J=2), 7.75 (1H, dd, J=8,2), 7.29 (1H, d, J=8), 4.20 (2H, q, J=7), 3.79 (2H, s), 2.43 (3H, s), 1.28 (3H, t, J=7).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05789408
Source datasetuspto-grants-1998_08
ORD IDord-32af1da76f094610a3a9f0b05e1bae04
Source noteuspto-grants-1998_08