참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,2-Dibromoethane | HCID 7839 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | 2-Ethyl-4-methoxypyrazolo[1,5-a]pyridine | HCID 21984578 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 7-Bromo-2-ethyl-4-methoxypyrazolo[1,5-a]pyridine | HCID 21984567 | — |
반응 단계
n-Butyllithium (1.31 mL) was slowly added dropwise to a solution of 2-ethyl-4-methoxypyrazolo[1,5-a]pyridine (303 mg) in tetrahydrofuran (15 mL) at −78° C. After stirring the mixture at −78° C. for 1 hour, 1,2-dibromoethane (0.18 mL) was added and stirring was continued for 1 hour. Saturated aqueous ammonium chloride was added, extraction was performed with ethyl acetate, the extract washed with brine and dried over magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was subjected to silica gel column chromatography (20 g), and the title compound (282 mg) was obtained from the n-hexane:ethyl acetate (5:1) fraction as a colorless oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07625925B2 |
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| 출처 데이터셋 | uspto-grants-2009_12 |
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| ORD ID | ord-36c761d88e6d4f768136cecaec694884 |
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| 출처 메모 | uspto-grants-2009_12 |
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