HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461830Generated: November 1, 2026
HCID 15020538, compound → HCID 14823451, compound
https://huagongshe.com/reaction/1461830
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 15020538 | HCID 15020538 | — |
| Reactant | Aluminum;lithium | HCID 16211445 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14823451 | HCID 14823451 | 81.1% |
Reaction Steps
To a stirred mixture of 4-[5-methoxy-1-phenylsulfonyl-1H-indazol-3-yl]-1-piperazinecarbonitrile (9.5 g, 0.0239 mol) in THF (150 ml) under N2 was added, dropwise, lithium aluminum [50 ml (2.1 eq) of a 1M LiAlH4 solution in THF]. After complete addition the reaction was warmed to reflux and stirred for 3 hours. To the cooled reaction was added carefully, H2O (15 ml) to destroy the excess LiAlH4. The mixture was allowed to stand overnight. The reaction mixture was filtered through a coarse sintered glass funnel. The resultant cake was washed well with THF and the THF filtrate was concentrated to afford 6.0 g, of a residue. The residue was triturated with ether and H2O and the resultant solid was collected and dried to afford 4.5 g of 5-methoxy-3-(1-piperazinyl)-1H-indazole, m.p. 163°-169° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05077405 |
|---|
| Source dataset | uspto-grants-1991_12 |
|---|
| ORD ID | ord-cf1fafa2038c45e6b7e2c244f7dd2651 |
|---|
| Source note | uspto-grants-1991_12 |
|---|