참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2,6-Difluoropyridine-4-boronic acid | HCID 2762747 | — |
| 반응물 | Cyclohexanol, 2-amino-, hydrochloride (1:1), (1R,2R)- | HCID 12228412 | — |
| 반응물 | 3-Iodooxetane | HCID 13356686 | — |
| 반응물 | Sodium hexamethyidisilazane | HCID 45051731 | — |
| 촉매 | Nickel(II) iodide | HCID 26038 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Isopropanol | HCID 3776 | — |
| 생성물 | 2,6-Difluoro-4-(oxetan-3-yl)pyridine | HCID 86707152 | 390% |
반응 단계
(2,6-difluoro-4-pyridyl)boronic acid (4.0004 mmol; 635.67 mg), Nickel(II) iodide (0.12001 mmol; 37.503 mg), Trans-2-aminocyclohexanol hydrochloride (0.12001 mmol; 18.382 mg), and Sodium hexamethyldisilazane (4.0004 mmol; 748.56 mg) were weighed into a CEM microwave vial. The mixture was capped then placed under a nitrogen atmosphere. Isopropanol (15 mL) was added and the mixture was stirred under nitrogen for 5 minutes. 3-Iodooxetane (2.0002 mmol; 368 mg) in Isopropanol (1.5 mL) was then added. The vial was heated at 100° C. under microwave for 20 minutes. The mixture was diluted with EtOH (15 mL) and filtered through Celite. The filter cake was washed with EtOH (2×10 mL). The mixture was concentrated and the residue was purified on silica eluted with 0 to 50% EtOAc in DCM to afford 2,6-difluoro-4-(oxetan-3-yl)pyridine (80.1 mg, 23%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09434725B2 |
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| 출처 데이터셋 | uspto-grants-2016_09 |
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| ORD ID | ord-fae1389599f34c52b589270d8994c3bd |
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| 출처 메모 | uspto-grants-2016_09 |
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