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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347792Generated: October 25, 2026

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

https://huagongshe.com/reaction/347792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylcarbodiimideHCID 12734—
ReactantSulfoacetic acidHCID 31257—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(4-Aminomethylphenyl)-1-(4-fluorophenyl)-3-[3-(4-fluorophenyl)-3-hydroxypropyl]azetidin-2-oneHCID 22252032—
ReactantHCID 178418300HCID 178418300—
SolventDimethylformamideHCID 6228—
Product(4-{1-(4-Fluorophenyl)-3-[3-(4-fluorophenyl)-3-hydroxypropyl]-4-oxoazetidin-2-yl}benzylcarbamoyl)methanesulfonic AcidHCID 21083138—

Reaction Steps

A solution of 120 mg of 4-(4-aminomethylphenyl)-1-(4-fluorophenyl)-3-[3-(4-fluorophenyl)-3-hydroxypropyl]azetidin-2-one (17), and 48 μl of diisopropylethylamine in 1 ml of dimethylformamide was added to a solution of 40 mg of sulfoacetic acid, 110 μl of diisopropylcarbodiimide, and 76 mg of hydroxybenzotriazole in 2 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 544.58 (C27H26F2N2O6S1); MS (ESI) 527.10 (M+H+—H2O)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176193B2
Source datasetuspto-grants-2007_02
ORD IDord-3e2da4d0ec654069983200b41eadd3b8
Source noteuspto-grants-2007_02