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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

反応式

関与物質

役割名称HCID仕込み量
反応物Acetamidine monohydrochlorideHCID 67170—
反応物N-{4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl}hydrazinecarboxamideHCID 820816—
溶媒DimethylformamideHCID 6228—
生成物2,4-dihydro-4-{4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl}-5-methyl-3H-1,2,4-triazol-3-oneHCID 12877040—

反応条件

温度130 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04267179
出典データセットuspto-grants-1981_05
ORD IDord-02a36d50c57b4e41811cf3f377a1d459
出典メモuspto-grants-1981_05