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HRID 614044作成日:2026年10月26日
Hydrazine hydrate (1:1) → 5-chloro-2-(3-glycylaminomethyl-5-methyl-4H-1,2,4-triazol-4-yl)-benzophenone hydrate
https://huagongshe.com/reaction/614044
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Hydrazine hydrate (1:1) | HCID 24654 | — |
| 反応物 | 5-chloro-2-[3-(2-phthalimidoacetamidomethyl)-5-methyl-4H-1,2,4-triazol-4-yl]-benzophenone | HCID 15567871 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 5-chloro-2-(3-glycylaminomethyl-5-methyl-4H-1,2,4-triazol-4-yl)-benzophenone hydrate | HCID 21325738 | 94% |
反応手順
To a solution of 5-chloro-2-[3-(2-phthalimidoacetamidomethyl)-5-methyl-4H-1,2,4-triazol-4-yl]-benzophenone (2.3 g) in ethanol (20 ml), hydrazine hydrate (0.92 g) is added, and the resultant mixture is refluxed for 1 hour. The precipitated phthalylhydrazide is filtered off, and the filtrate is evaporated under reduced pressure. The residue is dissolved in methylene chloride, washed with saturated aqueous sodium bicarbonate and water in order, dried over sodium sulfate, and evaporated under reduced pressure. The residue is chromatographed on a column of silica gel, and the product obtained from the eluate by evaporation is recrystallized from ethyl acetate to give 5-chloro-2-(3-glycylaminomethyl-5-methyl-4H-1,2,4-triazol-4-yl)-benzophenone hydrate as crystals melting at 110° to 113° C. The yield is 94%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04143048 |
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| 出典データセット | uspto-grants-1979_03 |
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| ORD ID | ord-4beb4fc9a79943b8b1fe5c5ca97e00c2 |
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| 出典メモ | uspto-grants-1979_03 |
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