참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Borane | HCID 6331 | — |
| 반응물 | 2,3-Dimethyl-1-butene | HCID 11249 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | InChI=1/C6H15B/c1-5(2)6(3,4)7/h5H,7H2,1-4H | HCID 5326179 | — |
| 반응물 | 3-methyl-6-vinyloxazolo[4,5-b]pyridin-2(3H)-one | HCID 19079286 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 6-(2-hydroxyethyl)-3-methyloxazolo[4,5-b]pyridin-2(3H)-one | HCID 19079317 | 78% |
반응 단계
A solution of boron hydride (1M in tetrahydrofuran) (5 ml, 5 mmol) is cooled using a salt/ice bath, and then 2,3-dimethyl-1-butene (0.6 ml, 5 mmol) are slowly added. The temperature of the solution is increased to 0° C. and stirring is maintained for a further 2 hours at that temperature. 3-methyl-6-vinyloxazolo[4,5-b]pyridin-2(3H)-one (1.14 mg, 5 mmol) dissolved in tetrahydrofuran (20 ml) is added to the previously prepared solution of thexylborane. The whole is stirred at 0° C. for 2 hours, then a 10% aqueous sodium hydroxide solution (2.40 ml) and also oxygenated water (2.00 ml) are added in succession. After 1 hour's stirring at room temperature and evaporation of the solvent under reduced pressure, the residue is taken up in water. Extraction is carried out with dichloromethane; the organic phase is dried over magnesium sulfate and filtered, and then the solvent is evaporated off under reduced pressure. Purification by flash chromatography on silica gel (eluant: dichloromethane/methanol: 95/5) yields 6-(2-hydroxyethyl)-3-methyloxazolo[4,5-b]pyridin-2(3H)-one in a yield of 78%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05767128 |
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| 출처 데이터셋 | uspto-grants-1998_06 |
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| ORD ID | ord-39ea5d17b9744646b760e50c6526fb59 |
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| 출처 메모 | uspto-grants-1998_06 |
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