HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164232Generated: October 26, 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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetamidine monohydrochloride | HCID 67170 | — |
| Reactant | N-{4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl}hydrazinecarboxamide | HCID 820816 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2,4-dihydro-4-{4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl}-5-methyl-3H-1,2,4-triazol-3-one | HCID 12877040 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04368200 |
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| Source dataset | uspto-grants-1983_01 |
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| ORD ID | ord-a0cbf9a02ecf4eb28a0bf733621c9a68 |
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| Source note | uspto-grants-1983_01 |
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