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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16197생성일: 2026년 10월 24일

Sodium Carbonate → N-(4-(6-(5-methylthiazol-2-ylamino)pyrazin-2-ylthio)phenyl)cyclopropanecarboxamide

https://huagongshe.com/ko/reaction/16197

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물2-Amino-5-methylthiazoleHCID 351770—
반응물1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
반응물N-(4-(6-chloropyrazin-2-ylthio)phenyl)cyclopropanecarboxamideHCID 59343401—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
용매1,4-DioxaneHCID 31275—
생성물N-(4-(6-(5-methylthiazol-2-ylamino)pyrazin-2-ylthio)phenyl)cyclopropanecarboxamideHCID 1595045314%

반응 조건

온도120 °C

반응 단계

To a solution of N-(4-(6-chloropyrazin-2-ylthio)phenyl)cyclopropanecarboxamide (0.82 mmol) and 2-amino-5-methylthiazole (0.86 mmol) in 1,4-dioxan (3 mL), 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (0.05 mmol), tris(dibenzylideneacetone)dipalladium (0.03 mmol) and sodium carbonate (1.15 mmol) were added. The resulting solution was heated at 120° C. in the microwave (175 W, 25 psi) for 3 h. Water (10 mL) and ethyl acetate (10 mL) were added and the layers separated. The aqueous layer was extracted further with ethyl acetate (2×10 mL), the combined organic layers dried (MgSO4) and concentrated in vacuo. The residue was purified by column chromatography eluting with MeOH:CH2Cl2 (1:20) to give the title compound (42.5 mg, 14%) as a light brown solid; 1H NMR (400 MHz, DMSO-d6) δ 0.81 (4H, m), 1.82 (1H, m), 2.16 (3H, s), 3.32 masked signal, 6.99 (1H, m), 7.58 (2H, m), 7.76 (2H, m), 7.84 (1H, s), 8.04 (1H, s), 10.49 (1H, s), 11.50 (1H, br s); MS (ES+): m/e=384.48 (100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737151B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-bd9ab69f0c3140b4b400eb9016653e04
출처 메모uspto-grants-2010_06