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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247965Generated: October 25, 2026

Pyridine → HCID 10049546, compound

https://huagongshe.com/reaction/247965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-PyridineethanamineHCID 75919—
Reactantp-TetradecyloxyphenylacetylchlorideHCID 10021844—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductHCID 10049546HCID 1004954644.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 0° C. solution of 5.24 g of 2-(2-aminoethyl)pyridine, 13.22 ml of pyridine and 50 ml of methylene chloride is added, dropwise, 15 g of product from Example 53 in 150 ml of methylene chloride. The reaction is stirred at 0° C. for 4 hours followed by 68 hours at room temperature. The reaction is diluted with chloroform, washed with saturated sodium bicarbonate, water and saturated sodium chloride, dried and concentrated in vacuo. The residue is purified by column chromatography (silica gel:75-100% ethyl acetate/hexane) to give 8.3 g of the desired product as colorless prisms.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05208247
Source datasetuspto-grants-1993_05
ORD IDord-60ee27cccad649b19c07e59f7e1a9480
Source noteuspto-grants-1993_05