참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | 1,2-Dibromo-1,1,2,2-tetrachloroethane | HCID 69426 | — |
| 반응물 | 2-Ethylpyrazolo[1,5-a]pyridine | HCID 16116261 | — |
| 반응물 | HCID 178418244 | HCID 178418244 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 7-Bromo-2-ethylpyrazolo[1,5-a]pyridine | HCID 21984510 | 73.1% |
반응 단계
After dissolving 2-ethylpyrazolo[1,5-a]pyridine (80 mg) in tetrahydrofuran (1 mL), an n-butyllithiumhexane solution (1.6 M; 0.58 mL) was added dropwise at −78° C. under a nitrogen stream, and the mixture was stirred for 30 minutes. A solution of 1,2-dibromo-1,1,2,2-tetrachloroethane (196 mg) in tetrahydrofuran (0.5 mL) was added to the reaction mixture, and stirring was continued for 30 minutes. The temperature was increased to room temperature, water was added, extraction was performed with ethyl acetate and the organic layer was washed with water and brine. After drying over anhydrous magnesium sulfate and filtration, the solvent was concentrated under reduced pressure, the residue was purified by silica gel column chromatography and the title compound (90 mg) was obtained from the n-hexane:ethyl acetate (20:1) fraction as a light brown oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07091215B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-2d57ba5cdf1547dca6908aa7dd81c8e7 |
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| 출처 메모 | uspto-grants-2006_08 |
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