참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | 4-Nitrobenzyl bromide | HCID 66011 | — |
| 반응물 | 1-(triphenylmethyl)-1H-Imidazole-4-acetic acid methyl ester | HCID 10523967 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 1-(4-Nitrophenylmethyl)-1H-imidazol-5-ylacetic acid methyl ester | HCID 70180988 | — |
반응 단계
To a solution of 1-(triphenylmethyl)-1H-imidazol-4-ylacetic acid methyl ester (23, 274 mg, 0.736 mmol) in acetonitrile (10 ml) was added 4-nitrobenzylbromide (159 mg, 0.736 mmol) and heated to 55° C. for 16 h. After this time, the reaction was cooled to room temperature, treated with ethyl acetate (20 ml) and the resulting precipitate was filtered. The filtrate was concentrated to dryness in vacuo and the residue was redissolved in acetonitrile (4 ml) and heated to 65° C. for 3 h. After this time, the reaction mixture was evaporated to dryness and combined with initial precipitate. This residue was dissolved in methanol (5 ml) and heated to reflux for 30 min. The resulting solution was evaporated in vacuo and the residue was purified by flash chromatography (2-5% methanol/methylene chloride gradient elution) to provide 16.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05652257 |
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| 출처 데이터셋 | uspto-grants-1997_07 |
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| ORD ID | ord-3fc800d25cf44c47acb266e7f13f3efd |
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| 출처 메모 | uspto-grants-1997_07 |
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