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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720859Generated: October 30, 2026

3-(Naphth-2-yl)acrylic acid → 3-(3-{[7-({(2R)-2-Hydroxy-2-[4-hydroxy-3-(hydroxymethyl)phenyl]ethyl}amino)heptyl]oxy}propyl)benzenesulfonamide (E)-3-(napthalen-2-yl)-2-propenoate

https://huagongshe.com/reaction/720859

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Naphth-2-yl)acrylic acidHCID 735835—
Reactant3-(3-{[7-({(2R)-2-Hydroxy-2-[4-hydroxy-3-(hydroxymethyl)phenyl]ethyl}amino)heptyl]oxy}propyl)benzenesulfonamideHCID 10289065—
SolventEthanolHCID 702—
Product3-(3-{[7-({(2R)-2-Hydroxy-2-[4-hydroxy-3-(hydroxymethyl)phenyl]ethyl}amino)heptyl]oxy}propyl)benzenesulfonamide (E)-3-(napthalen-2-yl)-2-propenoateHCID 86609643—

Reaction Steps

3-(3-{[7-({(2R)-2-Hydroxy-2-[4-hydroxy-3-(hydroxymethyl)phenyl]ethyl}amino)heptyl]oxy}propyl)benzenesulfonamide (1 g) was taken up in ethanol (6 ml) at room temperature with stirring and (E)-3-(napthalen-2-yl)-2-propenoic acid (0.39 g) added. The mixture was heated to ca 60° C. until a solution formed. The solution was cooled to room temperature and seed crystals of the title compound added. The mixture was aged for 65 h, the product filtered, washed with ethanol (1 ml) and dried to give the title compound (1.05 g) M Pt.=135° C.–146° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135600B2
Source datasetuspto-grants-2006_11
ORD IDord-080f25d6a676454191103d410294c293
Source noteuspto-grants-2006_11