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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 216151생성일: 2026년 10월 23일

Isopropanol → 4-Chloro-6-(3,4-dimethoxyphenyl)-2-(methylthio)pyrimidine

https://huagongshe.com/ko/reaction/216151

반응식

참여 물질

역할이름HCID투입량
반응물IsopropanolHCID 3776—
반응물Cesium carbonateHCID 10796—
반응물4,6-Dichloro-2-(methylthio)pyrimidineHCID 80531—
반응물3,4-Dimethoxyphenylboronic acidHCID 2734702—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물4-Chloro-6-(3,4-dimethoxyphenyl)-2-(methylthio)pyrimidineHCID 5763614683.6%

반응 조건

온도100 °C

반응 단계

Argon is bubbled through a mixture of 4,6-dichloro-2-(methylthio)pyrimidine [4.98 g, 25.55 mmol, Intermediate (29)], 3,4-dimethoxyphenylboronic acid [3.874 g, 21.29 mmol, Intermediate (32)], and Cs2CO3 (17.34 g, 53.23 mmol) in ethylene glycol dimethyl ether (56 mL) and water (14 mL), for a period of 15 minutes. To this mixture is added tetrakis(triphenylphosphine)palladium (0) (1.22 g, 1.06 mmol) the reaction vessel is heated to 100° C. After stirring overnight the mixture is diluted with water (250 mL) and extracted three times with EtOAc (100 mL). The organic extracts are combined, washed with brine (100 mL), and dried over magnesium sulfate. The mixture is filtered and concentrated to provide a solid that is dissolved in boiling isopropyl alcohol (40 mL) and allowed to cool to ambient temperature. After standing for 24 hours the solid is collected by filtration, washed with cold isopropyl alcohol and dried under high vacuum to afford 4-chloro-6-(3,4-dimethoxy-phenyl)-2-methylsulfanyl-pyrimidine [5.28 g, 83.5%, Intermediate (48)].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08193183B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-ebeec63bcd6a4bdfb9ce05b0a1a3d940
출처 메모uspto-grants-2012_06