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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704805Generated: October 31, 2026

3-(Oxiran-2-yl)pyridine → HCID 20073151, compound

https://huagongshe.com/reaction/704805

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Oxiran-2-yl)pyridineHCID 13319561—
Reactant5-(3-Aminobutyl)thiophene-2-carboxamideHCID 19809148—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 20073151HCID 200731519.3%

Reaction Steps

606 mg of 3-[(RS)-2-oxiranyl]pyridine and 991 mg of (RS)-5-(3-aminobutyl)-2-thiophenecarboxamide were heated to 100° for 25 hours in 5 ml of DMSO. The reaction mixture was diluted with water and extracted three times with methylene chloride. The methylene chloride solutions were washed with water, dried and evaporated in a vacuum. Chromatography of the residue on silica gel with ether/methanol gave 149 mg of 5-[(RS)-3-[[(RS)-2-hydroxy-2-(3-pyridyl)ethyl]amino]butyl]-2-thiophenecarboxamide, ε201 =14420; ε268 =11310.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04988714
Source datasetuspto-grants-1991_01
ORD IDord-7e4a9fe3eaa749cd9295e59a2048aa06
Source noteuspto-grants-1991_01