참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2,6-Dibromopyridine | HCID 12274 | — |
| 반응물 | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| 반응물 | 4-Hydroxypyrrolidine | HCID 98210 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-(6-Bromopyridin-2-yl)pyrrolidin-3-ol | HCID 21942298 | 100.9% |
반응 단계
A mixture of 5.7 g of 2,6-dibromopyridine, 2.5 g of 3-hydroxypyrrolidine, 3.6 ml of 1,8-diazabicyclo[5.4.0]-7-undecene (DBU) and 20 ml of tetrahydrofuran was heated under stirring under nitrogen atmosphere in an oil bath at 70° C. for 11 hours. The reaction mixture was separated with ethyl acetate-water. The organic layer was washed with water and brine, dried over anhydrous magnesium sulfate, and then concentrated. The residue was subjected to silicagel column chromatography with 10–30% ethyl acetate/hexane, to give 5.9 g of 2-bromo-6-(3-hydroxypyrrolidin-1-yl)pyridine.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07112593B2 |
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| 출처 데이터셋 | uspto-grants-2006_09 |
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| ORD ID | ord-5972ed998fd5418cb95cef454b659941 |
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| 출처 메모 | uspto-grants-2006_09 |
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