HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Fluconazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,1′-[2-(2,4-Difluorophenyl)-2-[(trimethylsilyl)oxy]-1,3-propanediyl]bis[1H-1,2,4-triazole] | HCID 11291888 | — |
| Solvent | Water | HCID 962 | — |
| Product | Fluconazole | HCID 3365 | 89% |
Reaction Steps
A mixture of 7.5 g (0.02 mol) of 2-(2,4-difluorophenyl)-1,3-bis(1,2,4-triazole-1-yl)-2-(trimethylsilyloxy)propane, 40 ml of methanol, 3 ml of water and 0.1 g of sodium hydroxide was stirred at room temperature for 1 h. After adding 300 ml of water the solution was concentrated to a volume of 50 ml with vacuum distillation. The obtained suspension was cooled to 0° C. and filtered. The obtained product was 6.12 g, water content was 11.5%. This was placed into a 100 ml flask and 0.1 g of crystal modification I of fluconazole seeding crystals were added thereto. The compound was dried on rotary evaporator at 80° C. for 3–4 h, until the weight was constant. 5.45 g of title compound was obtained. Yield: 87.4%. Mp.: 139–141° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07094904B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-480e5f12a0f94e4fa19353d5e0dfbe3c |
| Source note | uspto-grants-2006_08 |