참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Furan-3-boronic acid | HCID 2734358 | — |
| 반응물 | HCID 178432693 | HCID 178432693 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 4-(3-Chloro-phenylethynyl)-1-furan-3-yl-2-methyl-1H-imidazole | HCID 66879599 | — |
반응 단계
4-(3-Chloro-phenylethynyl)-2-methyl-1H-imidazole (200 mg, 0.92 mmol) was dissolved in 10 mL dichloromethane. Powdered molecular sieves (3 A, 200 mg), 3-furaneboronic acid (207 mg, 1.85 mmol) and [Cu(OH)TMEDA]2Cl2 (43 mg, 0.093 mmol) were added. Oxygen was bubbled through the reaction mixture for 10 minutes and stirring was continued at room temperature overnight. The reaction mixture was filtered through a dicalite speed plus pad and washed with 50 mL dichloromethane. The filtrate was washed with 50 mL water, dried with magnesium sulfate, filtered and evaporated. The crude product was purified by flash chromatography on silica gel (dichloromethane/methanol 100:0->90:10 gradient) and the desired compound was as a brown oil (21 mg, 8%), MS: m/e=283.1 (M+H+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07241760B2 |
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| 출처 데이터셋 | uspto-grants-2007_07 |
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| ORD ID | ord-90ea6191f94d4d1b9dd601134cd6cfc3 |
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| 출처 메모 | uspto-grants-2007_07 |
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