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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840195Generated: October 26, 2026

Ethyl Acetate → N-{(2R)-2-hydroxy-3-[(1-methyl-2,2-dioxo-2,3-dihydro-1H-2,1-benzisothiazol-5-yl)amino]propyl}acetamide

https://huagongshe.com/reaction/840195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantMagnesium trifluoromethanesulfonateHCID 2734125—
ReactantAcetamide, N-[(2S)-oxiranylmethyl]-HCID 11051615—
Reactant1-Methyl-5-nitro-1,3-dihydrobenzo[c]isothiazole 2,2-dioxideHCID 15538711—
SolventAcetonitrileHCID 6342—
SolventPalladiumHCID 23938—
ProductN-{(2R)-2-hydroxy-3-[(1-methyl-2,2-dioxo-2,3-dihydro-1H-2,1-benzisothiazol-5-yl)amino]propyl}acetamideHCID 1553871283.4%

Reaction Steps

The product of Step 1 (0.20 g, 0.88 mmol) is dissolved into EtOAc (30 mL) in a Parr bottle and 10% Pd/C (100 mg) added under nitrogen. The mixture is hydrogenated on a Parr apparatus for 2 hrs at 30 psi. Filtration and evaporation of solvent gave a white solid. This material is added to a mixture of N-[(2S)oxiranylmethyl] acetamide (0.81 g, 7.0 mmol) and magnesium trifluoromethanesulfonate (0.42 g, 1.3 mmol) in dry CH3CN (10 mL) at room temperature. After 20 hrs solvent is evaporated and the residue purified by chromatography (4%MeOH/CH2Cl2) to give a foamy solid (0.23 g, 79%). HRMS (FAB) calcd for C13H19N3O4S +H1 314.1174, found 314.1174.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06365612B2
Source datasetuspto-grants-2002_04
ORD IDord-cb73701bb7524c129e9fef26afd4297e
Source noteuspto-grants-2002_04