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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306251Generated: November 3, 2026

HCID 18433622, compound → HCID 18433566, compound

https://huagongshe.com/reaction/2306251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18433622HCID 18433622—
SolventEthanolHCID 702—
ProductHCID 18433566HCID 18433566—

Reaction Steps

3-(tert-Butyldimethylsilyloxy)-5-nitroquinoline, as described above in Step E, (4.58 g, 15.04 mmol) was dissolved in EtOH (150 mL) and EtOAc (150 mL), the vessel was degassed, Pd/C (0.458 g, 10 wt %) was added and the mixture was subjected to H2 (1 atm) with vigorous stirring for 1 hour. The mixture was filtered through a celite pad and concentrated in vacuo. The residue was chromatographed on silica gel, eluting with a gradient of 0% to 10% EtOAc in CH2Cl2, to yield the above-titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06441017B1
Source datasetuspto-grants-2002_08
ORD IDord-0a867fc34bf94d41b629140b36e30aee
Source noteuspto-grants-2002_08