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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methyltaurine | HCID 7882 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-[3-(4-Fluorophenyl)-3-hydroxypropyl]-1-[4-(4-fluorobutoxy)phenyl]-4-(4-methoxyphenyl)azetidin-2-one | HCID 21083137 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[(4-{4-[3-[3-(4-Fluorophenyl)-3-hydroxypropyl]-2-(4-methoxyphenyl)-4-oxoazetidin-1-yl]phenoxy}butyl)methylamino]ethylsulfonic Acid | HCID 12993300 | 31% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07176193B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-e21f9ce570a140b3a7662301042fa207 |
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| Source note | uspto-grants-2007_02 |
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