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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methanesulfonic Acid | HCID 6395 | — |
| 반응물 | 1,4-Dioxane | HCID 31275 | — |
| 반응물 | 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline | HCID 2734655 | — |
| 반응물 | 2-Chloro-4-methylpyrimidine | HCID 11629607 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 4-methyl-N-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrimidin-2-amine | HCID 58456319 | 58% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08551984B2 |
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| 출처 데이터셋 | uspto-grants-2013_10 |
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| ORD ID | ord-1e5a27bec4804b0e85c312736546e7de |
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| 출처 메모 | uspto-grants-2013_10 |
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