関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | N-Ethyltryptamine | HCID 6092 | — |
| 反応物 | Methyl 4-chloroformylbutyrate | HCID 73916 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | N-ethyl-N-(4-methoxycarbonylbutyryl)-tryptamine | HCID 23336475 | 74.4% |
反応手順
10 g of N-ethyl-tryptamine (i.e., 3-(2-ethylaminoethyl)-indole) were dissolved in 80 ml of pyridine, and 9.62 g of 4-methoxycarbonylbutyryl chloride were added dropwise thereto at 10° C. The mixture was stirred for one hour. After the reaction was completed, the mixture was acidified with dilute hydrochloric acid and then extracted with ethyl acetate. The extract was washed with water, an aqueous saturated sodium bicarbonate solution and water, successively. The washed extract was dried and evaporated under reduced pressure to remove solvent. The oily residue thus obtained was recrystallized from a mixture of ethanol and petroleum ether. 12.5 g of N-ethyl-N-(4-methoxycarbonylbutyryl)-tryptamine (i.e., 3-[2-(N-ethyl-4-methoxycarbonylbutanamido)ethyl]-indole]were thereby obtained as yellow crystals. M.p. 73°-75° C. Yield: 74.4%
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04228168 |
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| 出典データセット | uspto-grants-1980_10 |
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| ORD ID | ord-585b1100524d4a40a75b6c7e87f5f443 |
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| 出典メモ | uspto-grants-1980_10 |
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