HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → Lifarizine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Benzhydrylpiperazine | HCID 70048 | — |
| Reactant | HCID 22412164 | HCID 22412164 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | Lifarizine | HCID 71336 | — |
Reaction Steps
50 Grams (0.2 mol) of 2-(4-methylphenyl)-4-chloromethyl-5-methyl-1H-imidazole hydrochloride dissolved in 200 ml of a mixture of ethanol:water 6:4 were added dropwise to a refluxing solution of 55 grams (0.2 mol) of N-(diphenylmethyl)piperazine and 24 grams (0.6 mol) sodium hydroxide in 200 ml of a mixture of ethanol:water 6:4. After 2 to 3 hours 1-diphenylmethyl-4-[(2-(4-methylphenyl)-5-methyl-1H-imidazol-4-yl)methyl]piperazine precipitated from the reaction mixture. After having left the crystals standing at room temperature, they were removed by filtration and recrystallized from methanol to give the free base which melted at 220°-222° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05043447 |
| Source dataset | uspto-grants-1991_08 |
| ORD ID | ord-5e247f958bba46a3bb0b5270b612bc84 |
| Source note | uspto-grants-1991_08 |