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HRID 845245作成日:2026年10月26日
1,1'-Carbonyldiimidazole → 4-Methoxymethyl-5-morpholinomethyl-3-(3-ethyl,1,2,4-oxadiazol-5-yl)-beta-carboline
https://huagongshe.com/reaction/845245
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| 反応物 | N-Hydroxypropionimidamide | HCID 4092053 | — |
| 反応物 | 4-Methoxymethyl-5-(4-morpholinylmethyl)-beta-carboline-3-carboxylic acid | HCID 13850370 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 4-Methoxymethyl-5-morpholinomethyl-3-(3-ethyl,1,2,4-oxadiazol-5-yl)-beta-carboline | HCID 20132392 | 60.6% |
反応手順
A solution of 0.36 g of 4-methoxymethyl-5-morpholinomethyl-beta-carboline-3-carboxylic acid (prepared according to example 4) in 10 ml of absolute dimethylformamide is mixed with 0.2 g of carbonyldiimidazole and stirred for 30 minutes at 60° C. Then 0.4 g of propioamidoxime in 2 ml of DMF is added and the reaction mixture heated to 100° C. for 3 hours. After distilling off of the solvent in a vacuum, the residue is mixed with 20 ml of xylene and refluxed for 3 hours on the water separator, the reaction mixture is filtered hot, the filtrate is concentrated and chromatographed on silica gel. 0.25 g (60%) of oxadiazole derivative is obtained. Melting point 161°-163° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04757070 |
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| 出典データセット | uspto-grants-1988_07 |
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| ORD ID | ord-844a499bc1f2435293b62aada34c38da |
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| 出典メモ | uspto-grants-1988_07 |
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