Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1484939생성일: 2026년 10월 24일
Tributylvinyltin → N-tert-butyl-5-(4-(5-cyclopropyl-1H-pyrazol-3-ylamino)-5-vinylpyrimidin-2-yl)thiophene-2-sulfonamide
https://huagongshe.com/ko/reaction/1484939
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Tributylvinyltin | HCID 81998 | — |
| 반응물 | 5-(5-bromo-4-(5-cyclopropyl-1H-pyrazol-3-ylamino)pyrimidin-2-yl)-N-tert-butylthiophene-2-sulfonamide | HCID 58169355 | — |
| 촉매 | Tetrabutylammonium Bromide | HCID 74236 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | N-tert-butyl-5-(4-(5-cyclopropyl-1H-pyrazol-3-ylamino)-5-vinylpyrimidin-2-yl)thiophene-2-sulfonamide | HCID 58169328 | 84.9% |
반응 단계
The mixture of 5-(5-bromo-4-(5-cyclopropyl-1H-pyrazol-3-ylamino)pyrimidin-2-yl)-N-tert-butylthiophene-2-sulfonamide (1 g, 2.0 mmol, 1.0 eq), tributyl(vinyl)stannane (956 mg, 3.01 mmol, 1.5 eq), Pd (PPh3)2Cl2 (200 mg, 0.28 mmol, 0.14 eq) and Bu4NBr (642 mg, 2.0 mmol, 1.0 eq) in 1,4-dioxane (30 mL) was stirred at 100° C. for 2 h under N2, cooled to room temperature and partitioned between EtOAc and water. The organic layer was concentrated and purified by silica gel chromatography to afford N-tert-butyl-5-(4-(5-cyclopropyl-1H-pyrazol-3-ylamino)-5-vinylpyrimidin-2-yl)thiophene-2-sulfonamide (755 mg, 80%). LC-MS (m/z)=444 [M+H]+
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09422271B2 |
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| 출처 데이터셋 | uspto-grants-2016_08 |
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| ORD ID | ord-6ed90ddae5e54f75ad088b68f89fdc20 |
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| 출처 메모 | uspto-grants-2016_08 |
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