関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Morpholine | HCID 8083 | — |
| 反応物 | 3-Aminoquinoline | HCID 11375 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 2,4,6-Tribromopyrimidine | HCID 258580 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | N-(6-bromo-2-morpholinopyrimidin-4-yl)quinolin-3-amine | HCID 59507540 | — |
反応手順
To a solution of 2,4,6-tribromopyrimidine (5.40 g, 17.2 mmol) in acetonitrile (60 mL) was added quinolin-3-amine, followed by DIEA (8.99 mL, 51.6 mmol). The reaction mixture was heated to 45° C. overnight. Morpholine (1.50 mL, 17.2 mmol) was then added, and the reaction mixture continued heating for 4 h. The reaction mixture was then cooled to room temperature, concentrated and dissolved in EtOAc (about 500 mL), the organic solution was washed with saturated NaHCO3 (3×), H2O (2×), brine (1×) and dried over Na2SO4. The solution was then evaporated in the presence of silica gel and purified by column chromatography (SiO2, 15-25% EtOAc/Hexanes) to yield N-(6-bromo-2-morpholinopyrimidin-4-yl)quinolin-3-amine. LC/MS (m/z): 386.1 (MH+).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08563549B2 |
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| 出典データセット | uspto-grants-2013_10 |
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| ORD ID | ord-a424ee4c58394739ba3f92415541aba8 |
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| 出典メモ | uspto-grants-2013_10 |
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