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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347793Generated: October 25, 2026

Diisopropylcarbodiimide → {4-[3-[3-(4-Fluorophenyl)-3-hydroxypropyl]-2-(4-methoxyphenyl)-4-oxoazetidin-1-yl]benzylcarbamoyl}methanesulfonic Acid

https://huagongshe.com/reaction/347793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylcarbodiimideHCID 12734—
ReactantSulfoacetic acidHCID 31257—
Reactant1-(4-Aminomethylphenyl)-3-[3-(4-fluorophenyl)-3-hydroxypropyl]-4-(4-methoxyphenyl)azetidin-2-oneHCID 12111622—
ReactantHCID 178418300HCID 178418300—
SolventDimethylformamideHCID 6228—
Product{4-[3-[3-(4-Fluorophenyl)-3-hydroxypropyl]-2-(4-methoxyphenyl)-4-oxoazetidin-1-yl]benzylcarbamoyl}methanesulfonic AcidHCID 21083139—

Reaction Steps

A solution of 60 mg of 1-(4-aminomethylphenyl)-3-[3-(4-fluorophenyl)-3-hydroxypropyl]-4-(4-methoxyphenyl)azetidin-2-one (5) in 1 ml of dimethylformamide was added to a solution of 20 mg of sulfoacetic acid, 55 μl of diisopropylcarbodiimide, 38 mg of hydroxybenzotriazole in 1 ml of dimethylformamide, and the mixture was stirred at room temperature for 12 h. The reaction solution was concentrated and separated by HPLC (Knauer Eurospher-100-10-C18, water (0.1% trifluoroacetic acid)/acetonitrile (0.1% trifluoroacetic acid)=80/20->10/90). This gave the product of molecular weight 556.61 (C28H29F1N2O7S1); MS (ESI) 539.05 (M+H+—H2O)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176193B2
Source datasetuspto-grants-2007_02
ORD IDord-9a4a40a7f9414202b09b24ad98e8e7b2
Source noteuspto-grants-2007_02