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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

반응식

참여 물질

역할이름HCID투입량
반응물TributylvinyltinHCID 81998—
반응물5-(5-bromo-4-(5-cyclopropyl-1H-pyrazol-3-ylamino)pyrimidin-2-yl)-N-tert-butylthiophene-2-sulfonamideHCID 58169355—
촉매Tetrabutylammonium BromideHCID 74236—
용매1,4-DioxaneHCID 31275—
생성물N-tert-butyl-5-(4-(5-cyclopropyl-1H-pyrazol-3-ylamino)-5-vinylpyrimidin-2-yl)thiophene-2-sulfonamideHCID 5816932884.9%

반응 조건

온도100 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09422271B2
출처 데이터셋uspto-grants-2016_08
ORD IDord-6ed90ddae5e54f75ad088b68f89fdc20
출처 메모uspto-grants-2016_08