Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfolane | HCID 31347 | — |
| Reactant | HCID 15125488 | HCID 15125488 | — |
| Reactant | HCID 86743987 | HCID 86743987 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 15125489 | HCID 15125489 | — |
Reaction Steps
To a stirred mixture of 54.3 parts of 3-bromo-4-[4-(4-methoxyphenyl)-1-piperazinyl]-benzenamine and 189 parts of tetrahydrothiophene 1,1-dioxide was added portionwise, during a 30 minutes-period, 28.6 parts of ethyl[(dimethylamino)methylene]hydrazinecarboxylate at 160° C. Upon completion, stirring and heating were continued at 170° C. till all ethanol was distilled off. After cooling to room temperature, 120 parts of 4-methyl-2-pentanone were added to dissolve the sticky residue. The whole was heated till a solution was obtained. After cooling, the supernatant phase was decanted and the residue was stirred in 2,2'-oxybispropane. The product was filtered off and dried, yielding 44.6 parts of 4-[3-bromo-4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl]-2,4-dihydro-3H-1,2,4-triazol-3-one (int. 34).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04931444 |
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| Source dataset | uspto-grants-1990_06 |
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| ORD ID | ord-8c8eb1bdc06047fda7b5f930ca7a0547 |
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| Source note | uspto-grants-1990_06 |
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