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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Cesium carbonate | HCID 10796 | — |
| 반응물 | 1-Methylpiperazine | HCID 53167 | — |
| 반응물 | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| 반응물 | Ethyl 5-(3-bromobenzyl)-4-methylthiazole-2-carboxylate | HCID 86711480 | — |
| 촉매 | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | Ethyl 4-methyl-5-(3-(4-methylpiperazin-1-yl)benzyl)thiazole-2-carboxylate | HCID 86711481 | 75.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09115120B2 |
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| 출처 데이터셋 | uspto-grants-2015_08 |
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| ORD ID | ord-9d61ffea345d46baaee30779355c8b5e |
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| 출처 메모 | uspto-grants-2015_08 |
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