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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565704Generated: October 29, 2026

HCID 22111033, compound → HCID 22111010, compound

https://huagongshe.com/reaction/565704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22111033HCID 22111033—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 22111010HCID 2211101094.5%

Reaction Steps

To a solution of 1-[(5-amino-2,3dihydro-2,4,6,7-tetramethylbenzofuran-2-yl)methyl]-N-benzyl-N-(3,3-diphenylpropyl)-4-piperidinamine (1.5 g) in ethanol (50 mL) was added 0.30 g of 5% palladium on carbon (50% hydrous) and the mixture was stirred in a hydrogen atmosphere at 5 atmospheric pressure and 40° C. for 6 hours. This reaction mixture was filtered and the filtrate was concentrated under reduced pressure to provide 1.2 g of 1-[(5-amino-2,3-dihydro-2,4,6,7-tetramethylbenzofuran-2-yl)methyl]-N-(3,3-diphenylpropyl)-4-piperidinamine. Yield 94%. This product was treated with 4N-HCl solution in ethanol and the resulting trihydrochloride was recrystallized from ethanol/diethyl ether to provide 1.3 g of the title compound. Yield 82%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06172085B2
Source datasetuspto-grants-2001_01
ORD IDord-26467333e07a41aa8675c4b0aceaebc8
Source noteuspto-grants-2001_01