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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355628Generated: November 2, 2026

Hydrochloric Acid → HCID 59383097, compound

https://huagongshe.com/reaction/2355628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(3-Bromopropoxy)tetrahydro-2H-pyranHCID 2777988—
ReactantHCID 24854967HCID 24854967—
ReactantHCID 67399575HCID 67399575—
ReactantHCID 67400893HCID 67400893—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 59383097HCID 59383097—

Reaction Steps

The title compound was prepared in analogy to the procedure described for rac-4-{tert-butoxycarbonyl-[5-(2,2-dimethyl-[1,3]dioxolan-4-ylmethoxy)-pyridin-2-yl]-amino}-piperidine-1-carboxylic acid tert-butyl ester (intermediate B19/step 1) from 4-[tert-butoxycarbonyl-(5-hydroxy-pyridin-2-yl)-amino]-piperidine-1-carboxylic acid tert-butyl ester (intermediate B18 step 5) by reaction with rac-2-(3-bromopropoxy)-tetrahydro-2H-pyran (commercially available) and potassium carbonate in DMF at rt, followed by BOC and THP cleavage with 4 M HCl in dioxane and ethanol at 70° C. in analogy to the synthesis of (5-methanesulfonyl-pyridin-2-yl)-piperidin-4-yl-amine (intermediate B16/step 2). MS (ISP): 252.1 [M+H]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754744B2
Source datasetuspto-grants-2010_07
ORD IDord-bf7435c8ff494d3b91efd1e55e9f1fbd
Source noteuspto-grants-2010_07