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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 919573Generated: October 31, 2026

(R)-benzyl 3-((2-hydroxyethyl)(7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)piperidine-1-carboxylate → (R)-2-(piperidin-3-yl(7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)ethanol

https://huagongshe.com/reaction/919573

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-benzyl 3-((2-hydroxyethyl)(7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)piperidine-1-carboxylateHCID 69676530—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product(R)-2-(piperidin-3-yl(7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)ethanolHCID 69676526—

Reaction Steps

To a stirred solution of (R)-benzyl 3-((2-hydroxyethyl)(7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)piperidine-1-carboxylate (1.3 g, 2.4 mmol) in EtOH (10 mL) was added 10% Pd/C (0.8 g) under an atmosphere of N2 and the reaction was placed under an atmosphere of hydrogenated (1 atm.) for 2 h. The mixture was filtered through a celite pad and the filtrate was concentrated in vacuo to afford a residue which was used without further purification (0.9 g, 91%). LCMS [M+1]: 416.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273028B2
Source datasetuspto-grants-2016_03
ORD IDord-4e040aaf9f7346e8b567dec25cf98d76
Source noteuspto-grants-2016_03