HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1164232Erstellt: 26. Oktober 2026
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/1164232
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetamidine monohydrochloride | HCID 67170 | — |
| Edukt | N-{4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl}hydrazinecarboxamide | HCID 820816 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 2,4-dihydro-4-{4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl}-5-methyl-3H-1,2,4-triazol-3-one | HCID 12877040 | — |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04368200 |
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| Quelldatensatz | uspto-grants-1983_01 |
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| ORD ID | ord-a0cbf9a02ecf4eb28a0bf733621c9a68 |
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| Quellennotiz | uspto-grants-1983_01 |
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