Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 81250생성일: 2026년 10월 25일
Potassium Phosphate, Tribasic → 2-(prop-1-en-2-yl)-3H-imidazo[4,5-c]pyridine-6-carbonitrile
https://huagongshe.com/reaction/81250
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Potassium Phosphate, Tribasic | HCID 62657 | — |
| 반응물 | 4,4,5,5-Tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane | HCID 10997426 | — |
| 반응물 | 3H-imidazo[4,5-c]pyridine-6-carbonitrile | HCID 86724557 | — |
| 촉매 | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| 생성물 | 2-(prop-1-en-2-yl)-3H-imidazo[4,5-c]pyridine-6-carbonitrile | HCID 86724601 | — |
반응 단계
A vial was charged with the faster eluting enantiomer (enantiomer 1) of 2-bromo-4-(5-chloropyridin-3-yl)-3-[(1R or S)-1-(trans-4-methylcyclohexyl)ethyl]-3H-imidazo[4,5-c]pyridine-6-carbonitrile (Example 4.1, Step 3; 150 mg, 0.33 mmol), potassium phosphate (208 mg, 0.98 mmol), and [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (II) (23.9 mg, 0.033 mmol). The tube was evacuated and backfilled with argon (3×). Fully degassed dioxane (1.5 mL) and water (0.15 mL) were added, followed by 4,4,5,5-tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane (0.078 mL, 0.392 mmol). The vial was sealed and heated to 50° C. for 16 hours. The reaction mixture was cooled to room temperature and partitioned between water and ethyl acetate. The organic layer was dried over sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by silica gel chromatography (0-100% ethyl acetate/hexanes, linear gradient) to afford 4-(5-chloropyridin-3-yl)-3-[(1R or S)-1-(trans-4-methylcyclohexyl)ethyl]-2-(prop-1-en-2-yl)-3H-imidazo[4,5-c]pyridine-6-carbonitrile. MS ESI calc'd. for C24H26ClN5 [M+H]+ 420. found 420.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08846657B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-ab2ebf74fe0d4af79f492b8050273738 |
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| 출처 메모 | uspto-grants-2014_09 |
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