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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118170Generated: October 30, 2026

Ethyl isocyanate → 3-[4-({6-[(5R)-5-(2,2-Dimethyl-4H-1,3-benzodioxin-6-yl)-2-oxo-1,3-oxazolidin-3-yl]hexyl}oxy)butyl]-N-[(ethylamino)carbonyl]benzenesulfonamide

https://huagongshe.com/reaction/2118170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl isocyanateHCID 8022—
ReactantPotassium CarbonateHCID 11430—
Reactant3-[4-({6-[(5R)-5-(2,2-Dimethyl-4H-1,3-benzodioxin-6-yl)-2-oxo-1,3-oxazolidin-3-yl]hexyl}oxy)butyl]benzenesulfonamideHCID 42625249—
SolventAcetoneHCID 180—
Product3-[4-({6-[(5R)-5-(2,2-Dimethyl-4H-1,3-benzodioxin-6-yl)-2-oxo-1,3-oxazolidin-3-yl]hexyl}oxy)butyl]-N-[(ethylamino)carbonyl]benzenesulfonamideHCID 69197319—

Reaction Steps

Ethyl isocyanate (0.015 g) was added to a stirred mixture of 3-[4-({6-[(5R)-5-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-2-oxo-1,3-oxazolidin-3-yl]hexyl}oxy)butyl]benzenesulfonamide (0.11 g) and K2CO3 (0.055 g) in acetone (2 ml). The mixture was heated at reflux for 2 h then ethyl isocyanate (0.005 g) was added. After 0.5 h the reaction mixture was cooled and quenched with water (1 ml). The mixture was partitioned between EtOAc (20 ml) and H2O (20 ml). The aqueous phase was extracted with EtOAc (20 ml). The combined EtOAc phases were washed with brine (10 ml) then dried (Na2SO4) and concentrated. The residue was purified by SPE (silica 5 g) with

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442836B2
Source datasetuspto-grants-2008_10
ORD IDord-6c770bfbde0745109ebfd7a8e401b471
Source noteuspto-grants-2008_10