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1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → (3,4,5,6-Tetrahydroxytetrahydropyran-2-ylmethyl)10,12-tricosadiynoate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| 反応物 | 10,12-Tricosadiynoic Acid | HCID 538457 | — |
| 反応物 | 1,2:3,4-Di-O-isopropylidene-alpha-D-galactopyranose | HCID 2723629 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | (3,4,5,6-Tetrahydroxytetrahydropyran-2-ylmethyl)10,12-tricosadiynoate | HCID 53883249 | — |
反応手順
1,2;3,4-di-O-isopropylidene-D-galactopyranose (2.6 g, 10 mmol) and 10,12-tricosadiynoic acid (3.5 g, 10 mmol) were dissolved in 25 ml methylene chloride. 1-Ethyl-3(3-dimethylaminopropyl)carbodiimide (2 g, >10 mmol) was added neat. The reaction mixture was stirred overnight at room temperature. The reaction mixture was diluted to 100 ml, extracted with water (2×25 ml), dried over MgSO4 and the solvent was removed in vacuo. The crude product was treated with trifluoroacetic acid (10 ml) at room temperature for 30 minutes, evaporated in vacuo, and purified by straight phase chromatography on a CHROMATOTRON, eluted with methanol/chloroform (5:95). The product was characterised by NMR.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05567413 |
| 出典データセット | uspto-grants-1996_10 |
| ORD ID | ord-99c35bd0113f409aadcc4e2cb047536f |
| 出典メモ | uspto-grants-1996_10 |