HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Benzenesulfonyl)-3-(4-methylpiperazin-1-yl)-1H-indazole → 3-(4-Methylpiperazin-1-yl)-1H-indazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Benzenesulfonyl)-3-(4-methylpiperazin-1-yl)-1H-indazole | HCID 14823425 | — |
| Reactant | HCID 178418582 | HCID 178418582 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(4-Methylpiperazin-1-yl)-1H-indazole | HCID 14823452 | 80.3% |
Reaction Steps
A stirred mixture of 3-(4-methyl-1-piperazinyl)-1-phenylsulfonyl-1H-indazole (13.5 g, 38 mmol), methanol (150 ml) and 25% CH3ONa in methanol (15.3 ml) was stirred and refluxed for 2.5 hours. The reaction was concentrated to about one-tenth its volume, and water was added to the mixture, resulting in a red solution. The solution was extracted with dichloromethane, the extract washed (H2O), dried (MgSO4), and the solvent was concentrated to afford 6.6 g of a rose-colored solid. Two recrystallizations from toluenehexane afforded 4.3 g (52%) of 3-(4-methyl-1-piperazinyl)-1H-indazole as an off-white solid, m.p.=111-113° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06043240 |
| Source dataset | uspto-grants-2000_03 |
| ORD ID | ord-6a8ff4c7fe8d40099f1b751465213688 |
| Source note | uspto-grants-2000_03 |