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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347789Generated: October 26, 2026

N-Methyltaurine → 2-[(4-{4-[3-[3-(4-Fluorophenyl)-3-hydroxypropyl]-2-(4-methoxyphenyl)-4-oxoazetidin-1-yl]phenoxy}butyl)methylamino]ethylsulfonic Acid

https://huagongshe.com/reaction/347789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethyltaurineHCID 7882—
ReactantPotassium CarbonateHCID 11430—
Reactant3-[3-(4-Fluorophenyl)-3-hydroxypropyl]-1-[4-(4-fluorobutoxy)phenyl]-4-(4-methoxyphenyl)azetidin-2-oneHCID 21083137—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-[(4-{4-[3-[3-(4-Fluorophenyl)-3-hydroxypropyl]-2-(4-methoxyphenyl)-4-oxoazetidin-1-yl]phenoxy}butyl)methylamino]ethylsulfonic AcidHCID 1299330031%

Reaction Conditions

Temperature50 °C

Reaction Steps

130 mg of 3-[3-(4-fluorophenyl)-3-hydroxypropyl]-1-[4-(4-fluorobutoxy)phenyl]-4-(4-methoxyphenyl)azetidin-2-one (7) were dissolved in 6 ml of absolute methanol. 120 mg of N-methyltaurine in 2 ml of water and 60 mg of potassium carbonate were then added. The mixture was stirred at 50° C. for 24 h. The reaction mixture was concentrated using a rotary evaporator and the residue was purified by preparative chromatography. Freeze-drying gave the product (50 mg) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176193B2
Source datasetuspto-grants-2007_02
ORD IDord-e21f9ce570a140b3a7662301042fa207
Source noteuspto-grants-2007_02