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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874094Generated: October 29, 2026

Pyridine → HCID 23093540, compound

https://huagongshe.com/reaction/874094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactantp-Anisoyl chlorideHCID 7477—
ReactantN-(tert-Butoxycarbonyl)-N-methyl-2-aminoethanolHCID 545700—
SolventEthyl AcetateHCID 8857—
ProductHCID 23093540HCID 2309354081.1%

Reaction Steps

To a mixture of tert-butyl 2-hydroxyethyl(methyl)carbamate (1.75 g) obtained in Reference Example 1 and ethyl acetate (10 mL) were added 4-methoxybenzoyl chloride (1.88 g) and pyridine (0.97 mL). After stirring at room temperature for 14 hrs., 4-methoxybenzoyl chloride (0.70 g) and pyridine (0.97 mL) were added and the mixture was stirred at room temperature for 1 hr. Ethyl acetate (80 mL) was added to the reaction mixture, and the mixture was washed with water (20 mL), a saturated aqueous sodium hydrogen carbonate solution (20 mL) and water (20 mL), and dried over anhydrous magnesium sulfate. After concentration under reduced pressure, the residue was dissolved in ethyl acetate (10 mL), and a 4N hydrogen chloride—ethyl acetate solution (10 mL) was added. After stirring at room temperature for 1 hr., diethyl ether (20 mL) was added, and the precipitated solid was collected by filtration. The solid was washed twice with ethyl acetate (15 mL) and dried under reduced pressure at 60° C. to give the title compound (1.99 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980322B2
Source datasetuspto-grants-2015_03
ORD IDord-3aa54c8bc9c14674937e7324e1cad4e6
Source noteuspto-grants-2015_03