참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | 2-Amino-5-methylpyridine | HCID 15348 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | Trimethylaluminum hexane | HCID 86584505 | — |
| 반응물 | HCID 178499199 | HCID 178499199 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | HCID 178426582 | HCID 178426582 | 61.6% |
반응 단계
2-Amino-5-methylpyridine (81 mg) is dissolved in chloroform (5 ml). After adding 0.98 M trimethyl aluminum-hexane solution (763 μl) under ice-cooling, the reaction solution is stirred under ice-cooling for 10 minutes, and then at room temperature for 0.5 hours. To the resulting reaction solution is added methyl 3-({[trans-4-(3-oxomorpholin-4-yl)cyclohexyl]carbonyl}amino)furo[3,2-b]pyridine-2-carboxylate (150 mg) obtained in Reference Example 79, and the mixture is stirred at room temperature for 2 hours and at 50° C. under heating for 5 hours. To the reaction solution is added 10% hydrochloric acid (3 ml) under ice-cooling, and the mixture is stirred at room temperature for 0.5 hours. The reaction solution is then neutralized by adding saturated aqueous sodium hydrogen carbonate solution, and extracted with chloroform. The organic layer is washed with saturated brine, dried over sodium sulfate, and the solvent is evaporated under reduced pressure. The residue is purified by NH-silica gel column chromatography (eluent: ethyl acetate followed by ethyl acetate/methanol=10/1). The resulting solid is suspended in diethyl ether, and collected by filtration to give the title compound (110 mg).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07737161B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-eae17f8ebaf8493a9c5aabf38ce0cd74 |
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| 출처 메모 | uspto-grants-2010_06 |
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