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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1532567생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1532567

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 H11) are initially introduced into 35 ml of N-methylpyrrolidone. After addition of 13.0 g of potassium carbonate, the mixture is stirred and heated up to 55° C. 2.36 ml of methyl iodide in 5.0 ml of N-methylpyrrolidone are then slowly added dropwise. After the mixture has been subsequently stirred for 2 hours, diethyl ether and water are added, the mixture is extracted by shaking and the organic phase is separated off. The ether phase which has been separated off is washed with brine, dried over sodium sulfate, filtered and concentrated. The crude product is purified by means of flash chromatography (silica gel; eluting agent: toluene/ethyl acetate 100/1). First, 3.96 g of the isomeric 5-pyridylpyrazole (yield 42%) are isolated as a yellow oil, and then 1.96 g of the 3-pyridylpyrazoie (yield 21%) are isolated as a yellow solid. The Rf values of the two isomeric 3- and 5-pyridyipyrazoles are as follows on silica gel 60 F254 with toluenelethyl acetate 30/1 as the eluting agent (UV):

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06204221B1
출처 데이터셋uspto-grants-2001_03
ORD IDord-69a9b53d7d414033b6c8974eb2ef21d4
출처 메모uspto-grants-2001_03