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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725312Generated: October 26, 2026

N-Methyltaurine → 2-{[4-(4-{1-(4-Fluorophenyl)-3-[3-(4-fluorophenyl)-3-hydroxypropyl]-4-oxoazetidin-2-yl}phenoxy)butyl]methylamino}ethanesulfonic acid

https://huagongshe.com/reaction/1725312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethyltaurineHCID 7882—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(4-Fluorophenyl)-3-[3-(4-fluorophenyl)-hydroxypropyl]-4-[4-(4-iodobutoxy)phenyl]azetidin-2-oneHCID 22252048—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-{[4-(4-{1-(4-Fluorophenyl)-3-[3-(4-fluorophenyl)-3-hydroxypropyl]-4-oxoazetidin-2-yl}phenoxy)butyl]methylamino}ethanesulfonic acidHCID 23593512—

Reaction Conditions

Temperature50 °C

Reaction Steps

64.5 mg of 1-(4-fluorophenyl)-3-[3-(4-fluorophenyl)-hydroxypropyl]-4-[4-(4-iodobutoxy)phenyl]azetidin-2-one are dissolved in 3 ml of methanol. 60.7 mg of 2-methylaminoethanesulfonic acid are then dissolved in 1 ml of water, and 30.4 mg of potassium carbonate are added. The reaction is stirred at 50° C. for 8 h. After concentration using a rotary evaporator at 40° C., the residue is passed over a reverse-phase cartridge (methanol). The resulting crude product is dissolved in hot methanol. The precipitate formed on cooling is filtered off, and the mother liquor is concentrated using a rotary evaporator. The product is obtained as an oil. C31H36F2N2O6S (602) MS (ESI): M+-18

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07488829B2
Source datasetuspto-grants-2009_02
ORD IDord-c36d8096c1474509a03bf36b70dd7d09
Source noteuspto-grants-2009_02