Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096037Generated: October 31, 2026

Pyridine → HCID 23093540, compound

https://huagongshe.com/reaction/2096037

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 Synthetic 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) was further added, and stirred at room temperature for 1 hr. To the reaction solution was added ethyl acetate (80 mL), and washed sequentially with water (20 mL), saturated aqueous solution of sodium bicarbonate (20 mL) and water (20 mL), and dried over anhydrous magnesium sulfate. The solution was concentrated under reduced pressure, and the residue was dissolved in ethyl acetate (10 mL), followed by adding 4N hydrogen chloride-ethyl acetate solution (10 mL). After stirring at room temperature for 1 hr, diethyl ether (20 mL) was added, and the depositting solid was collected by filtration. The solid was washed twice with ethyl acetate (15 mL), and dried at 60° C. under reduced pressure to give title compound as white solid (1.99 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08449911B2
Source datasetuspto-grants-2013_05
ORD IDord-178c7a87b26c4ee4aeb339b10eb74b6e
Source noteuspto-grants-2013_05