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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1621388생성일: 2026년 10월 26일

4-Chloro-6-methyl-1,3,5-triazin-2-amine → 4-(2-Fluoro-5-methylpyridin-3-yl)-6-methyl-1,3,5-triazin-2-amine

https://huagongshe.com/reaction/1621388

반응식

참여 물질

역할이름HCID투입량
반응물4-Chloro-6-methyl-1,3,5-triazin-2-amineHCID 30591—
반응물1,4-DioxaneHCID 31275—
반응물Potassium AcetateHCID 517044—
반응물2-Fluoro-5-methylpyridine-3-boronic acidHCID 44754858—
촉매Bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II)HCID 11714597—
생성물4-(2-Fluoro-5-methylpyridin-3-yl)-6-methyl-1,3,5-triazin-2-amineHCID 6015471841%

반응 조건

온도120 °C

반응 단계

1,4-Dioxane (3.00 mL, 8.5 mmol) was added to a mixture of bis(di-tert-butyl (4-dimethylaminophenyl)phosphine)dichloropalladium(II) (Aldrich, St. Louis, Mo.) (0.27 g, 0.43 mmol), 2-fluoro-5-methylpyridin-3-ylboronic acid (1.6 g, 10 mmol), 4-chloro-6-methyl-1,3,5-triazin-2-amine (1.24 g, 8.5 mmol) and potassium acetate (2.5 g, 26 mmol) and the mixture was sealed and heated at 120° C. for 30 min under microwave irradiation. After cooling, the mixture was passed through a short plug of Celite® (diatomaceous earth). The filter cake was washed with DCM (3×20 mL). The combined organic phases were concentrated. Flash column chromatographic purification (short column, SiO2, pure DCM to 5% MeOH in DCM) provided 4-(2-fluoro-5-methylpyridin-3-yl)-6-methyl-1,3,5-triazin-2-amine (0.76, 41%) as a white solid which was used for the next step. LCMS (API-ES) m/z 220 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08772480B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-775a6bcf56494f58bf8e9eb74a7a2fbe
출처 메모uspto-grants-2014_07