Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 79349생성일: 2026년 10월 24일
Phosphorus sulfide (P2S5) → N-(3-ethyl-1-((6-methylpyridin-2-yl)methyl)-1H-indazol-4-yl)-7-(1,3,4-thiadiazol-2-yl)imidazo[1,2-a]pyridine-3-carboxamide
https://huagongshe.com/ko/reaction/79349
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Phosphorus sulfide (P2S5) | HCID 14817 | — |
| 반응물 | Hexamethyldisiloxane | HCID 24764 | — |
| 반응물 | N-(3-ethyl-1-((6-methylpyridin-2-yl)methyl)-1H-indazol-4-yl)-7-(2-formylhydrazinecarbonyl)imidazo[1,2-a]pyridine-3-carboxamide | HCID 67260976 | — |
| 용매 | Dioxane toluene | HCID 21840791 | — |
| 생성물 | N-(3-ethyl-1-((6-methylpyridin-2-yl)methyl)-1H-indazol-4-yl)-7-(1,3,4-thiadiazol-2-yl)imidazo[1,2-a]pyridine-3-carboxamide | HCID 53262089 | 4.2% |
반응 단계
To N-(3-ethyl-1-((6-methylpyridin-2-yl)methyl)-1H-indazol-4-yl)-7-(2-formylhydrazinecarbonyl)imidazo[1,2-a]pyridine-3-carboxamide (36 mg, 0.073 mmol) in toluene/dioxane (1 mL/1 mL) was added hexamethyldisiloxane (71 mg, 0.44 mmol) and P2S5 (81 mg, 0.36 mmol). The reaction mixture was sealed and heated in a microwave reactor to 110° C. for 3 hours. The mixture was then concentrated under reduced pressure and the residue was purified by silica gel chromatography (DCM/MeOH 10:1) to provide the final product (1.5 mg). MS (ES+APCI) m/z=495 (M+H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08841455B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-e51ef1358ef948d0ac0002c2f20a5bd7 |
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| 출처 메모 | uspto-grants-2014_09 |
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