関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethanol | HCID 702 | — |
| 反応物 | Carbon Disulfide | HCID 6348 | — |
| 反応物 | Benzyl Bromide | HCID 7498 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | D-1,2,3,4-Tetrahydronorharman-3-carboxylic acid | HCID 675102 | — |
| 生成物 | (3R)-2-[(Benzylthio)thiocarbonyl]-1,2,3,4-tetrahydro-beta-carboline-3-carboxylic acid | HCID 13561931 | — |
反応手順
To a mixture of (3R)-1,2,3,4-tetrahydro-β-carboline-3-carboxylic acid (5.4 g), 2N NaOH (25 ml) and 50% ethanol (70 ml) is added dropwise carbon disulfide (1.5 ml) at room temperature. The mixture is stirred at room temperature for 30 minutes, and thereto is added dropwise benzyl bromide (3.5 ml), and the mixture is further stirred at the same temperature for 3 hours and then distilled to remover the solvent. To the residue is added water, and the mixture is extracted with ether. The aqueous layer is acidified with 10% HCl, extracted with ethyl acetate. The extract is washed with water, dried and distilled to remove the solvent. The residue is purified by silica gel column chromatography (solvent, chloroform:methanol=20:1) to give the title compound (4.5 g) as pale yellow powder.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04628057 |
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| 出典データセット | uspto-grants-1986_12 |
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| ORD ID | ord-0271a25bd06d4969a382bfb50786e4d6 |
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| 出典メモ | uspto-grants-1986_12 |
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