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HRID 1877502생성일: 2026년 10월 27일

Triethylamine → 2-Cyano-5-fluoro-3-(tetrahydropyran-4-yl)aminopyridine

https://huagongshe.com/reaction/1877502

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Potassium CarbonateHCID 11430—
반응물2-Cyano-3,5-difluoropyridineHCID 2783253—
반응물4-Aminotetrahydropyran hydrochlorideHCID 44118693—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물2-Cyano-5-fluoro-3-(tetrahydropyran-4-yl)aminopyridineHCID 6701670525.3%

반응 조건

온도115 °C

반응 단계

200 mg of 2-cyano-3,5-difluoropyridine, 236 mg of 4-aminotetrahydropyran hydrochloride, 395 mg of potassium carbonate and 173.4 mg of triethylamine in 3 ml of dimethyl sulphoxide are introduced into a 5 ml microwave tube reactor. The mixture is then heated in a microwave for 1 hour at 115° C. The reaction medium is run into 50 ml of water and 50 ml of ethyl acetate. The aqueous phase is re-extracted twice with 25 ml of ethyl acetate. The combined organic phases are washed with water and then with a saturated aqueous solution of sodium chloride, dried over sodium sulphate and concentrated under reduced pressure. After purification by flash chromatography on 25 g of silica gel, elution being carried out with mixtures of ethyl acetate and heptane (40/60 then 60/40 by volume), and the first eluted product being recovered, 80 mg of 2-cyano-5-fluoro-3-(tetrahydropyran-4-yl)aminopyridine are thus obtained in the form of an ecru powder, the characteristics of which are the following:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08309721B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-8beba0a0506647ada78e1492031e6961
출처 메모uspto-grants-2012_11