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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454638Generated: October 30, 2026

HCID 66990342, compound → HCID 58508727, compound

https://huagongshe.com/reaction/454638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66990342HCID 66990342—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 58508727HCID 5850872765.8%

Reaction Steps

To a solution mixture of the obtained tert-butyl 2-(2-(benzyloxy)-5-(2-(4-methylpiperazin-1-yl)ethyl)benzamido)-4-phenylbenzoate (0.10 g) in methanol (1.5 mL) and ethyl acetate (1.5 mL), 10% palladium-carbon (0.10 g) was added, followed by stirring under a hydrogen atmosphere at room temperature for 1 hour. The insoluble substance was removed by filtration, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography [Kanto Chemical Co., Inc., silica gel 60 (spherical), eluent: 100-90% chloroform/methanol] to obtain 0.056 g of tert-butyl 2-(2-hydroxy-5-(2-(4-methylpiperazin-1-yl)ethyl)benzamido)-4-phenylbenzoate as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492582B2
Source datasetuspto-grants-2013_07
ORD IDord-3311b3d6b4da45ec86513d5ae7c4148f
Source noteuspto-grants-2013_07