참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | 4-bromo-3-nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazole | HCID 66652794 | — |
| 반응물 | 4-bromo-5-nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazole | HCID 66653152 | — |
| 반응물 | HCID 66655615 | HCID 66655615 | — |
| 촉매 | HCID 178418397 | HCID 178418397 | — |
| 용매 | 1,2-Dimethoxyethane | HCID 8071 | — |
| 용매 | Potassium Carbonate | HCID 11430 | — |
| 생성물 | HCID 66652937 | HCID 66652937 | — |
반응 단계
To a solution of 2-hydroxy-5-(trifluoromethoxy)phenylboronic acid (Preparation 23, 20.5 g, 92.4 mmol) and 4-bromo-3-nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazole or 4-bromo-5-nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazole (Preparation 22, 22.7 g, 82.2 mmol) in 1,2-dimethoxyethane (300 mL) and 2 M potassium carbonate in water (117 mL, 212 mmol) was added tetrakis(triphenylphosphine)palladium(0) (5.0 g, 4.3 mmol). The solution was sparged with argon (×3) and heated at 80° C. for 8 hours. The reaction mixture was cooled to ambient temperature and the layers separated. The aqueous phase was washed with ethyl acetate (×2). The combined organic phase was dried over anhydrous magnesium sulfate and concentrated in vacuo. The residue was purified by silica gel column chromatography (0 to 30% ethyl acetate in hexanes gradient elution) and concentrated in vacuo. Excess hexanes was added to the residue and the resulting solid was collected by filtration and dried in vacuo to afford the title compound as off white crystals (19.5 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09145407B2 |
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| 출처 데이터셋 | uspto-grants-2015_09 |
|---|
| ORD ID | ord-1ef9ecefa3de4463937a3de935c4744e |
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| 출처 메모 | uspto-grants-2015_09 |
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