HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formic Acid → 4-formyl-1-(1-phenyl-1H-indazol-3-yl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 1-phenyl-3-(1-piperazinyl)-1H-indazole | HCID 9795644 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-formyl-1-(1-phenyl-1H-indazol-3-yl)piperazine | HCID 15117098 | 42% |
Reaction Steps
To a solution of 3.4 ml of acetic anhydride and 1.5 ml of formic acid heated at 55° C. for 1.5 hours and then cooled to ambient temperature was added, dropwise, a solution of 5.6 g of 1-phenyl-3-(1-piperazinyl)-1H-indazole in 20 ml of tetrahydrofuran. The reaction mixture was stirred at ambient temperature for 2 hours and then concentrated to an oil. Trituration of the oil with refluxing diethyl ether yielded a solid which was recrystallized from isopropanol (3×) to yield 2.6 g (42%) of 4-formyl-1-(1-phenyl-1H-indazol-3-yl)piperazine, m.p. 130°-132°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04999356 |
| Source dataset | uspto-grants-1991_03 |
| ORD ID | ord-b6f36608343d49b6acdc80ac0c09f714 |
| Source note | uspto-grants-1991_03 |