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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 650482생성일: 2026년 10월 23일

Diethyl Ether → 2-(1H-Pyrazol-3-Yl)Pyridine

https://huagongshe.com/ko/reaction/650482

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물Methyl iodideHCID 6328—
반응물Potassium CarbonateHCID 11430—
반응물HCID 21712162HCID 21712162—
용매WaterHCID 962—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물2-(1H-Pyrazol-3-Yl)PyridineHCID 279765786.6%

반응 조건

온도55 °C

반응 단계

8.88 g of 3-(3,5-dichloro-2-pyridyl)-5-trifluoromethyl-[1H]-pyrazole (Example P10) are introduced into 35 ml of N-methylpyrrolidone. After the addition of 13.0 g of potassium carbonate, the mixture is stirred and heated to 55° C. 2.36 ml of methyl iodide in 5.0 ml of N-methylpyrrolidone are then slowly added dropwise. After subsequently stirring for 2 hours, diethyl ether and water are added, the mixture is extracted by shaking and the organic phase is separated off. The separated ethereal phase is washed with brine, dried over sodium sulfate, filtered and concentrated. The crude product is purified by means of flash chromatography (silica gel; eluant: toluene/ethyl acetate 100/1). First of all 3.96 g of the 5-pyridylpyrazole isomer (yield 42%) are isolated in the form of a yellow oil and then 1.96 g of the 3-pyridylpyrazole (yield 21%) are isolated in the form of a yellow solid. The Rf values of the 3- and 5-pyridylpyrazole isomers on silica gel 60 F254 using toluene/ethyl acetate 30/1 as eluant (UV) are:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06274536B1
출처 데이터셋uspto-grants-2001_08
ORD IDord-092cbf3cb2f146188c66b0197eb7263b
출처 메모uspto-grants-2001_08