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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 501437생성일: 2026년 10월 24일

Hexachloroethane → 3-(2-Butynyl)-2,4-dichloro-3H-imidazo[4,5-c]pyridine

https://huagongshe.com/ko/reaction/501437

반응식

참여 물질

역할이름HCID투입량
반응물HexachloroethaneHCID 6214—
반응물Ammonium ChlorideHCID 25517—
반응물Lithium diisopropylamideHCID 2724682—
반응물3-(2-Butynyl)-4-chloro-3H-imidazo[4,5-c]pyridineHCID 23070729—
용매TetrahydrofuranHCID 8028—
생성물3-(2-Butynyl)-2,4-dichloro-3H-imidazo[4,5-c]pyridineHCID 2307098021%

반응 단계

2.22 ml of a tetrahydrofuran solution of lithium diisopropylamide was added dropwise to a 5 ml tetrahydrofuran solution of 490 mg of 3-(2-butynyl)-4-chloro-3H-imidazo[4,5-c]pyridine in a dry ice-methanol bath, and the mixture was stirred below −66° C. for 20 minutes. The resulting reaction mixture was added dropwise to a 2 ml tetrahydrofuran solution of 1.13 g of hexachloroethane while the temperature of the mixture was controlled to be −63° C. or lower. The mixture was stirred for one hour and 40 minutes in the same bath, and then a saturated aqueous ammonium chloride solution was added thereto. The resulting mixture was extracted twice with ethyl acetate, and the organic layer was dried over anhydrous magnesium sulfate, then filtered. The filtrate was concentrated under reduced pressure. Then, the resulting residue was purified by silica gel column chromatography. Thus, 120 mg of brown oily material was obtained from the fraction eluted with hexane-ethyl acetate (2:1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07772226B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-8adadceae381408d99ea7a971222e9dd
출처 메모uspto-grants-2010_08