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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 517540생성일: 2026년 10월 25일

Cesium carbonate → Ethyl 4-methyl-5-(3-(4-methylpiperazin-1-yl)benzyl)thiazole-2-carboxylate

https://huagongshe.com/reaction/517540

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물1-MethylpiperazineHCID 53167—
반응물2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
반응물Ethyl 5-(3-bromobenzyl)-4-methylthiazole-2-carboxylateHCID 86711480—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TolueneHCID 1140—
생성물Ethyl 4-methyl-5-(3-(4-methylpiperazin-1-yl)benzyl)thiazole-2-carboxylateHCID 8671148175.1%

반응 단계

A mixture of ethyl 5-(3-bromobenzyl)-4-methylthiazole-2-carboxylate (340 mg, 1.0 mmol), 1-methylpiperazine (0.2 mL, 2 mmol) and Cs2CO3 (652 mg, 2 mmol) in toluene (5 mL) was degassed (argon bubbling for 5 min), tris(dibenzylideneacetone)dipalladium(0) (46 mg, 0.05 mmol) and 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl (48 mg, 0.1 mmol) were quickly added. The reaction mixture was refluxed overnight, cooled to RT, then quenched with H2O and extracted with EtOAc (3×30 mL). The organic layers were washed with H2O (30 mL) and brine (10 mL), dried over Na2SO4, filtered, and concentrated to afford the crude product, which was purified by silica gel column chromatography (DCM:MeOH=20:1) to give ethyl 4-methyl-5-(3-(4-methylpiperazin-1-yl)benzyl)thiazole-2-carboxylate as a yellow solid (270 mg, 75%). MS (ES+) C19H25N3O2S requires: 359, found: 360[M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09115120B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-9d61ffea345d46baaee30779355c8b5e
출처 메모uspto-grants-2015_08