돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 464104생성일: 2026년 10월 25일

Water → 5-Amino-4-cyano-1-(5-trimethylsilyl-4-pentynyl)pyrazole

https://huagongshe.com/reaction/464104

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물5-Amino-4-cyanopyrazoleHCID 85515—
반응물Silane, (5-iodo-1-pentynyl)trimethyl-HCID 11140046—
용매ChloroformHCID 6212—
용매DimethylformamideHCID 6228—
생성물5-Amino-4-cyano-1-(5-trimethylsilyl-4-pentynyl)pyrazoleHCID 2026383320.4%

반응 단계

A suspension of 5-amino-4-cyanopyrazole (10 g) and finely ground anhydrous potassium carbonate (38 g) in dry DMF (100 ml) was treated with 5-iodo-1-trimethylsilyl-1-pentyne (25 g) and the mixture was stirred under nitrogen for two days at room temperature. The reaction mixture was then poured into water and the product extracted into ethyl acetate. The extract was washed with water and then with brine, dried over Na2SO4, and evaporated to give a semisolid brown residue. This solid was taken up in chloroform and filtered through a short plug of silica gel. Evaporation of the chloroform left a tan solid comprising a mixture of the isomeric compounds 5-amino-4-cyano-1-(5-trimethylsilyl-4-pentynyl)pyrazole and 3-amino-4-cyano-1-(5-trimethylsilyl-4-pentynyl)pyrazole. Fractional recrystallization from ethyl acetate/hexane gave 4.66 grams of the desired 5-amino-4-cyano-1-(5-trimethylsilyl-4-pentynyl)pyrazole: mp 125°-127°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04546104
출처 데이터셋uspto-grants-1985_10
ORD IDord-0bebbb73c7e44a5eadcc029bcc5de8fb
출처 메모uspto-grants-1985_10