HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109642Generated: October 30, 2026
HCID 10296324, compound → HCID 21959454, compound
https://huagongshe.com/reaction/2109642
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 10296324 | HCID 10296324 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21959454 | HCID 21959454 | — |
Reaction Steps
The title compound was prepared from N-(4-tert-butyl-3-nitro-phenyl)-2-(1H-indazol-6-ylamino)-nicotinamide by dissolving in EtOH (20 ml) and adding Sn(II)Cl2 (12.58 g) and stirred at RT for 5 h and at 0° C. overnight. The mix was warmed to RT and quenched by pouring onto ice, neutralized with NaHCO3 and basified with 6N NAOH. An emulsion formed upon addition of EtOAc which was filtered through Celite® and the aqueous layer was extracted with EtOAc. The combined organic layers were washed with H2O, brine and dried over MgSO4 then purified by flash chromatography (3-5% MeOH to afford the product as a orange-yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07514564B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-fde5f0fab103472dac11c581d8989a78 |
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| Source note | uspto-grants-2009_04 |
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