참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Hydrazine hydrate (1:1) | HCID 24654 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 6-Phenylhexan-1-amine | HCID 145558 | — |
| 반응물 | N-(6-phenylhexyl)phthalimide | HCID 19599919 | — |
| 반응물 | Methyl 2-(2-mesyloxyethyl)furan-3-carboxylate | HCID 19600087 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 5-(6-phenylhexyl)-6,7-dihydro-5H-furo[3,2-c]pyridin-4-one | HCID 19600108 | — |
반응 단계
A solution of the above crude methyl 2-(2-mesyloxyethyl)furan-3-carboxylate, crude 6-phenylhexylamine [prepared by refluxing a solution of 1.79 g (5.81 mmol) of N-(6-phenylhexyl)phthalimide and 0.28 ml (5.8 mmol) of hydrazine monohydrate in 20 ml of ethanol for 1 hour, cooling the reaction mixture to room temperature, then pouring it into aqueous sodium hydroxide, extracting with ethyl acetate 3 times, drying the combined organic layer over anhydrous magnesium sulfate, and distilling off the solvent] and 2.02 ml (11.6 mmol) of N,N-diisopropylethylamine in 50 ml of acetonitrile was refluxed for 3 days. The reaction mixture was poured into water and extracted with ethyl acetate 3 times. The combined organic layer was dried over anhydrous magnesium sulfate; the solvent was distilled off under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane/ethyl acetate=6/1 to 3/1) to yield the desired product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05998433 |
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| 출처 데이터셋 | uspto-grants-1999_12 |
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| ORD ID | ord-c054cf3d45ef429785556fdf86b4affa |
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| 출처 메모 | uspto-grants-1999_12 |
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