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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | 6-bromo-2-(2-ethylsulfanylphenyl)-3-methyl-3H-imidazo[4,5-b]pyridine | HCID 67982033 | — |
| 촉매 | Zinc cyanide (Zn(CN)2) | HCID 11186 | — |
| 촉매 | HCID 178418397 | HCID 178418397 | — |
| 생성물 | 6-cyano-2-(2-ethylsulfanylphenyl)-3-methyl-3H-imidazo[4,5-b]pyridine | HCID 86708206 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08853238B2 |
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| 출처 데이터셋 | uspto-grants-2014_10 |
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| ORD ID | ord-a3a8327606074f2aa3ea857af3cd42cf |
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| 출처 메모 | uspto-grants-2014_10 |
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