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HRID 2286556作成日:2026年10月26日
Acetamidine monohydrochloride → 2,4-dihydro-4-{4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl}-5-methyl-3H-1,2,4-triazol-3-one
https://huagongshe.com/reaction/2286556
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetamidine monohydrochloride | HCID 67170 | — |
| 反応物 | N-{4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl}hydrazinecarboxamide | HCID 820816 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 2,4-dihydro-4-{4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl}-5-methyl-3H-1,2,4-triazol-3-one | HCID 12877040 | — |
反応手順
A mixture of 53 parts of N-{4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl}hydrazinecarboxamide, 53 parts of ethanimidamide hydrochloride and 135 parts of N,N-dimethylformamide is stirred and heated for 3 hours at 130° C. The reaction mixture is cooled and poured onto water. The precipitated product is filtered off, washed with water and with methanol, and crystallized from N,N-dimethylformamide. The product is filtered off and recrystallized from 1,4-dioxane, yielding 19.5 parts of 2,4-dihydro-4-{4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl}-5-methyl-3H-1,2,4-triazol-3-one; 298.4° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04267179 |
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| 出典データセット | uspto-grants-1981_05 |
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| ORD ID | ord-02a36d50c57b4e41811cf3f377a1d459 |
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| 出典メモ | uspto-grants-1981_05 |
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