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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480475Generated: October 31, 2026

HCID 86722694, compound → HCID 178520492, compound

https://huagongshe.com/reaction/1480475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86722694HCID 86722694—
ReactantHCID 178418361HCID 178418361—
SolventEthanolHCID 702—
ProductHCID 178520492HCID 178520492—

Reaction Steps

3,5-dichlorobenzyl 4-(3-(((1-benzyl-1H-1,2,3-triazol-4-yl)methyl)amino)-3-oxopropyl)piperidine-1-carboxylate (51 mg, 0.096 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. After 90 mins the solution was concentrated and the residue purified using preparative LC-MS. Product fractions were collected, concentrated under reduced pressure, diluted with ethyl acetate, and extracted with water. The organics were 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-5fa5c6f6632c4a11900d1fa960f16e68
Source noteuspto-grants-2016_08