참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pyrazole | HCID 1048 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 5-Bromo-1,3-difluoro-2-nitrobenzene | HCID 21335487 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | HCID 67004648 | HCID 67004648 | 86% |
반응 단계
To a suspension of sodium hydride (44 mg, 1.1 mmol, 60% oil dispersion) in THF (4 mL), stirred at 0° C., was added a solution of pyrazole (72 mg, 1.05 mmol) in THF (1 mL). The resulting mixture was stirred at 0° C. for 5 minutes and a solution of 5-bromo-1,3-difluoro-2-nitro-benzene (238 mg, 1 mmol) in THF (1 mL) was added. The mixture was stirred at room temperature for 1 hour, quenched by addition of water (1 mL), then partitioned between water (20 mL) and ethyl acetate (50 mL). The organic layer was washed with brine, dried (MgSO4), and concentrated in vacuo. The residue was purified by column chromatography over silica gel eluted with ethyl acetate:hexanes (1:6), to afford 240 mg (86%) of the title compound. 1H NMR (CDCl3) δ 6.55 (t, 1H), 7.45 (d, 1H), 7.60 (s, 1H), 7.80 (m, 2H). MS M+1 287, M+1+2 289.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08193352B2 |
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| 출처 데이터셋 | uspto-grants-2012_06 |
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| ORD ID | ord-18cf073f84af497e87c3739ab11ab8f0 |
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| 출처 메모 | uspto-grants-2012_06 |
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