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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1626798Generated: November 1, 2026

Hydrochloric Acid → HCID 68196368, compound

https://huagongshe.com/reaction/1626798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHexaneHCID 8058—
ReactantEthyl AcetateHCID 8857—
Reactant1,4-DioxaneHCID 31275—
ReactantHCID 86670084HCID 86670084—
ProductHCID 68196368HCID 6819636844%

Reaction Steps

Benzyl({[5-(benzyloxy)-2-{[1-(4-{5-[1-(methoxymethoxy)ethyl]pyridin-2-yl}phenyl)piperidin-4-yl]methyl}-6-methylpyrimidin-4-yl]carbonyl}amino)acetate (0.80 g, 1.1 mmol) was dissolved in ethyl acetate (6 mL), and a solution of hydrogen chloride in dioxane (4 M, 1.5 mL, 6.0 mmol) was added, followed by stirring at room temperature for 1.5 hours. After hexane was added to the reaction solution, the deposited solid was collected by filtration using hexane. To this, was added a saturated aqueous sodium hydrogencarbonate solution, followed by extraction with ethyl acetate, and subsequently the organic layer was concentrated under reduced pressure. The resulting residue was purified by chromatography on a silica gel column (Moritex Corporation, elution solvent: hexane/ethyl acetate), and a fraction corresponding to the Rf value=0.30 (hexane/ethyl acetate=1/1) by thin layer chromatography was concentrated under reduced pressure to afford the title compound (0.32 g, 0.49 mmol) as a yellow solid (yield 44%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785462B2
Source datasetuspto-grants-2014_07
ORD IDord-c6a7ef3c5ba04a24aa0d508a3ce32095
Source noteuspto-grants-2014_07