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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096042Generated: November 2, 2026

Pyridine → HCID 23103069, compound

https://huagongshe.com/reaction/2096042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzoyl chloride, 3,4,5-trimethoxy-HCID 78282—
ReactantN-(tert-Butoxycarbonyl)-N-methyl-2-aminoethanolHCID 545700—
SolventEthyl AcetateHCID 8857—
ProductHCID 23103069HCID 2310306958.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a mixture of tert-butyl 2-hydroxyethyl(methyl)carbamate (1.75 g) obtained in Reference Synthetic Example 1 and ethyl acetate (10 mL) were added 3,4,5-trimethoxybenzoyl chloride (2.54 g) and pyridine (0.97 mL). After stirring at 60° C. for 14 hrs, to the reaction solution were further added 3,4,5-trimethoxybenzoyl chloride (1.30 g), pyridine (0.97 mL) and ethyl acetate (10 mL), and stirred at 60° C. for 24 hrs. The reaction solution was filtered, and to the filtrate were added ethyl acetate (50 mL) and water (30 mL). After separating the layers, the ethyl acetate layer was washed sequentially with 1 N hydrochloric acid (30 mL), water (30 mL), aqueous solution of copper (II) sulfate (30 mL), water (30 mL) and saturated brine (30 mL), followed by drying over anhydrous magnesium sulfate. The solution was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (elute with ethyl acetate:hexane=1:1). To the purified materials was added 4N hydrogen chloride-ethyl acetate solution (10 mL). After stirring at room temperature for 4 hrs, the solution was concentrated under reduced pressure. Toluene (10 mL) was added to the residue, and concentrated under reduced pressure. The residue was suspended in ethyl acetate, and the solid was collected by filtration. After washing with ethyl acetate (15 mL), the solid was dried under reduced pressure to give title compound as white solid (1.79 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08449911B2
Source datasetuspto-grants-2013_05
ORD IDord-cd5192bfccac4aa08184d38407a1e3c0
Source noteuspto-grants-2013_05