돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 533611생성일: 2026년 10월 27일

N-methyl-2-pyrrolidone → 6-cyano-2-(2-ethylsulfanylphenyl)-3-methyl-3H-imidazo[4,5-b]pyridine

https://huagongshe.com/reaction/533611

반응식

참여 물질

역할이름HCID투입량
반응물N-methyl-2-pyrrolidoneHCID 13387—
반응물Ammonium ChlorideHCID 25517—
반응물6-bromo-2-(2-ethylsulfanylphenyl)-3-methyl-3H-imidazo[4,5-b]pyridineHCID 67982033—
촉매Zinc cyanide (Zn(CN)2)HCID 11186—
촉매HCID 178418397HCID 178418397—
생성물6-cyano-2-(2-ethylsulfanylphenyl)-3-methyl-3H-imidazo[4,5-b]pyridineHCID 86708206—

반응 조건

온도90 °C

반응 단계

A mixture of zinc cyanide (0.47 g), tetrakis(triphenylphosphine)palladium (0.12 g), 6-bromo-2-(2-ethylsulfanylphenyl)-3-methyl-3H-imidazo[4,5-b]pyridine (0.70 g), and N-methylpyrrolidone (hereinafter referred to as NMP) (4 ml) was stirred at 90° C. for 2 hours. Into the reaction mixture cooled to room temperature, saturated aqueous ammonium chloride solution was poured, and extracted with ethyl acetate. The organic layer was dried over sodium sulfate, and concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography to give 0.59 g of 6-cyano-2-(2-ethylsulfanylphenyl)-3-methyl-3H-imidazo[4,5-b]pyridine (hereinafter referred to as Present Compound 48).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08853238B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-a3a8327606074f2aa3ea857af3cd42cf
출처 메모uspto-grants-2014_10