참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Boron tribromide | HCID 25134 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | 4-(4-methoxy-benzenesulfonyl)-3,4-dihydro-2H-pyrido[4,3-b][1,4]oxazine | HCID 66936616 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 4-(2,3-Dihydro-pyrido[4,3-b][1,4]oxazin-4-sulfonyl)-phenol | HCID 44608376 | 56.2% |
반응 단계
In a 100 ml flask, 4-(4-methoxy-benzenesulfonyl)-3,4-dihydro-2H-pyrido[4,3-b][1,4]oxazine (699 mg, 2.282 mmol) was dissolved in dichloromethane (30 ml) and the mixture was cooled to 0□. 1.0M Boron tribromide dissolved in dichloromethane (11.4 ml, 11.4 mmol) was added thereto and stirred at room temperature for 16 hours. After neutralizing with saturated solution of sodium hydrogen carbonate to pH 8 to 9, the mixture was adjusted to pH 6 again by using 1N hydrochloric acid and extracted with dichloromethane. The combined organic layer was washed with saturated saline solution and dried over anhydrous sodium sulfate (Na2SO4), filtered and evaporated under reduced pressure. The residue was purified by column chromatography on silica eluting with a solvent of methanol:dichloromethane=1:20. The fractions containing the product were collected and evaporated to obtain white solid (375 mg, 56.2%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08394792B2 |
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| 출처 데이터셋 | uspto-grants-2013_03 |
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| ORD ID | ord-8b44fec77661458f8dae130767dce7fa |
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| 출처 메모 | uspto-grants-2013_03 |
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