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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 449864생성일: 2026년 10월 24일

2-Aminothiazole → 2,6-dichloro-N-(2-(thiazol-2-ylamino)pyridin-4-yl)benzamide

https://huagongshe.com/ko/reaction/449864

반응식

참여 물질

역할이름HCID투입량
반응물2-AminothiazoleHCID 2155—
반응물Cesium carbonateHCID 10796—
반응물1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
반응물N-(2-Bromopyridin-4-yl)-2,6-dichlorobenzamideHCID 75464886—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매1,4-DioxaneHCID 31275—
생성물2,6-dichloro-N-(2-(thiazol-2-ylamino)pyridin-4-yl)benzamideHCID 5961824625.3%

반응 조건

온도80 °C

반응 단계

A 25 mL microwave tube containing N-(2-bromopyridin-4-yl)-2,6-dichlorobenzamide (0.21 g, 0.61 mmol), 2-aminothiazole (92 mg, 0.92 mmol), Pd2(dba)3 (56 mg, 0.061 mmol), Cs2CO3 (0.4 g, 1.22 mmol), 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (Xantphos, 71 mg, 0.122 mmol), and dioxane (8 mL) was degassed and then charged with N2 (3×). The resulting mixture was heated at 80° C. overnight. After cooling, the mixture was diluted with dioxane (20 mL) and filtered through celite. The filtrate was concentrated under reduced pressure and the residue was purified by reverse-phase HPLC (Gemini, 200 mm×25 mm, gradient: CH3CN/0.05% NH3.H2O, 50-80, 10 min) to afford the desired product (56.4 mg, yield: 25%). 1HNMR: (DMSO-d6, 400 MHz): 611.26 (s, 1H), 11.13 (s, 1H), 8.21 (d, J=6.0 Hz, 1H), 7.61-7.50 (m, 4H), 7.36 (d, J=3.6 Hz, 1H), 7.11 (q, J=1.6, 6.0 Hz, 1H), 6.98 (d, J=3.6 Hz, 1H). LCMS (ESI) m/z: 364.8 [M+H+]

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08486950B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-3118848d6bdc46cebe46f27181f6a3d1
출처 메모uspto-grants-2013_07