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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916801Generated: October 30, 2026

HCID 11478544, compound → HCID 69384227, compound

https://huagongshe.com/reaction/916801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11478544HCID 11478544—
ReactantHCID 178431339HCID 178431339—
ReactantHCID 178504318HCID 178504318—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69384227HCID 69384227—

Reaction Conditions

Temperature75 °C

Reaction Steps

The mixture of N-(3-{[2-(4-{2-[(5R)-5-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-2-oxo-1,3-oxazolidin-3-yl]ethyl}phenoxy)ethoxy]methyl}phenyl)urea and N-(3-{[2-(4-{2-[(5R)-5-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-2-oxo-1,3-oxazolidin-3-yl]ethyl}phenoxy)ethoxy]methyl}phenyl)dicarbonimidic diamide (135 mg) in THF (2 mL) was treated with KOSiMe3 (123 mg) and the resulting solution was heated at 75° C. under nitrogen for 1.5 h. The reaction mixture was then quenched with MeOH and concentrated in vacuo. The residue was taken up in EtOAc, washed with water, dried (MgSO4) and concentrated in vacuo. The residue was purified by HPLC to give N-[3-({2-[4-(2-{[(2R)-2-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-2-hydroxyethyl]amino}ethyl)phenoxy]ethoxy}methyl)phenyl]urea (12 mg). LCMS RT=2.47 min and N-[3-([2-[4-(2-{[(2R)-2-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-2-hydroxyethyl]amino}ethyl)phenoxy]ethoxy}methyl)phenyl]dicarbonimidic diamide (6 mg). LCMS RT=2.58 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07271197B2
Source datasetuspto-grants-2007_09
ORD IDord-208d42b73de649a9823b160b11ec8242
Source noteuspto-grants-2007_09