HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → Itraconazole Hydroxy Isopropyltriazolone Impurity
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 2,4-dihydro-4-[4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl]-2-(1-methylethyl)-3H-1,2,4-triazol-3-one | HCID 14855350 | — |
| Solvent | Water | HCID 962 | — |
| Product | Itraconazole Hydroxy Isopropyltriazolone Impurity | HCID 14855351 | 86% |
Reaction Steps
A mixture of 4.7 parts of 2,4-dihydro-4-[4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl]-2-(1-methylethyl)-3H-1,2,4-triazol-3-one and 75 parts of a hydrobromic acid solution 48% in water was stirred and refluxed for 3 hours. The reaction mixture was evaporated and the residue was dissolved in a mixture of methanol and water. The whole was neutralized with a sodium hydrogen carbonate solution and the product was extracted with trichloromethane. The extract was dried, filtered and evaporated. The residue was triturated in 2-propanol, yielding 3.9 parts (86%) of 2,4-dihydro-4-[4-[4-(4-hydroxyphenyl)-1-piperazinyl]phenyl]-2-(1-methylethyl)-3H-1,2,4-triazol-3-one, mp. 208.4° C. (intermediate 10).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04916134 |
| Source dataset | uspto-grants-1990_04 |
| ORD ID | ord-759cd2de2bdc4c5b80b3c43d94bb2975 |
| Source note | uspto-grants-1990_04 |