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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109642Generated: October 30, 2026

HCID 10296324, compound → HCID 21959454, compound

https://huagongshe.com/reaction/2109642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10296324HCID 10296324—
SolventEthanolHCID 702—
ProductHCID 21959454HCID 21959454—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514564B2
Source datasetuspto-grants-2009_04
ORD IDord-fde5f0fab103472dac11c581d8989a78
Source noteuspto-grants-2009_04