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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1039887생성일: 2026년 10월 26일

Methanesulfonic Acid → 4-methyl-N-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrimidin-2-amine

https://huagongshe.com/reaction/1039887

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonic AcidHCID 6395—
반응물1,4-DioxaneHCID 31275—
반응물3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 2734655—
반응물2-Chloro-4-methylpyrimidineHCID 11629607—
용매Ethyl AcetateHCID 8857—
생성물4-methyl-N-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrimidin-2-amineHCID 5845631958%

반응 조건

온도100 °C

반응 단계

To a flask containing 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline (1.50 g, 6.85 mmol) and 2-chloro-4-methylpyrimidine (1.01 g, 7.87 mmol) were added dioxane (69 mL) and methanesulfonic acid (0.51 mL, 7.87 mmol). The reaction was heated at 100° C. overnight. The reaction was then cooled to room temperature, diluted with ethyl acetate, washed with water, dried over magnesium sulfate, filtered and concentrated. Flash chromatography was used for purification to yield 4-methyl-N-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]pyrimidin-2-amine (1.23 g, 3.95 mmol, 58% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08551984B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-1e5a27bec4804b0e85c312736546e7de
출처 메모uspto-grants-2013_10