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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480479Generated: November 1, 2026

HCID 86722696, compound → HCID 178520321, compound

https://huagongshe.com/reaction/1480479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86722696HCID 86722696—
ReactantHCID 178418361HCID 178418361—
SolventEthanolHCID 702—
ProductHCID 178520321HCID 178520321—

Reaction Steps

3,5-dichlorobenzyl 4-(2-((2-(1-benzyl-1H-1,2,3-triazol-4-yl)ethyl)amino)-2-oxoethyl)piperidine-1-carboxylate (81.5 mg, 0.154 mmol) was dissolved in ethanol (4 ml). The solution was then submitted to continuous flow hydrogenation using H-cube hydrogenation apparatus, at 70° C. and 30 bar hydrogen pressure for 2 hours. The resultant solution was concentrated under reduced pressure. Purification was carried out using preparative LC-MS. Product fractions were collected, concentrated under reduced pressure, diluted with ethyl acetate, and washed with water. The organic portion was separated, dried over MgSO4, filtered, and concentrated under reduced pressure to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409895B2
Source datasetuspto-grants-2016_08
ORD IDord-2831194b7c564d6fbb62a026556a34e3
Source noteuspto-grants-2016_08