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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2110663생성일: 2026년 10월 26일

Sodium Carbonate → [2-(2-Chloro-6-fluoro-phenyl)-ethyl]-[6-(6-methoxy-pyridin-3-yl)-2-methylsulfanyl-pyrimidin-4-yl]-amine

https://huagongshe.com/reaction/2110663

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물2-(2-Chloro-6-fluorophenyl)ethan-1-amineHCID 2734094—
반응물4-Chloro-6-(6-methoxy-pyridin-3-yl)-2-methylsulfanyl-pyrimidineHCID 57636137—
용매WaterHCID 962—
용매1-MethylpyrrolidineHCID 8454—
생성물[2-(2-Chloro-6-fluoro-phenyl)-ethyl]-[6-(6-methoxy-pyridin-3-yl)-2-methylsulfanyl-pyrimidin-4-yl]-amineHCID 1155321094.5%

반응 조건

온도175 °C

반응 단계

A mixture of 2-(2-chloro-6-fluoro-phenyl)-ethylamine [1.02 g, 5.88 mmol, Intermediate (23)], Na2CO3 (1.65 g, 19.6 mmol), and 4-chloro-6-(6-methoxy-pyridin-3-yl)-2-methylsulfanyl-pyrimidine [1.05 g, 3.92 mmol, Intermediate (38)] in N-methyl pyrrolidine (10 mL), is heated to 175° C. for 3 hours. The reaction mixture is diluted with water, and extracted with ethyl acetate. The extracts are washed with water, dried over magnesium sulfate, filtered, and concentrated. The residue is subjected to short-path chromatography on silica gel eluting with EtOAc to afford [2-(2-chloro-6-fluoro-phenyl)-ethyl]-[6-(6-methoxy-pyridin-3-yl)-2-methylsulfanyl-pyrimidin-4-yl]-amine [1.5 g, Example 30]. LCMS: RT=3.37 minutes, MS: 405 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07517889B2
출처 데이터셋uspto-grants-2009_04
ORD IDord-07b927087b194c79b4bd062a3d27ea5f
출처 메모uspto-grants-2009_04