HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → N-{(2R)-2-hydroxy-3-[(1-methyl-2,2-dioxo-2,3-dihydro-1H-2,1-benzisothiazol-5-yl)amino]propyl}acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Magnesium trifluoromethanesulfonate | HCID 2734125 | — |
| Reactant | Acetamide, N-[(2S)-oxiranylmethyl]- | HCID 11051615 | — |
| Reactant | 1-Methyl-5-nitro-1,3-dihydrobenzo[c]isothiazole 2,2-dioxide | HCID 15538711 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Palladium | HCID 23938 | — |
| Product | N-{(2R)-2-hydroxy-3-[(1-methyl-2,2-dioxo-2,3-dihydro-1H-2,1-benzisothiazol-5-yl)amino]propyl}acetamide | HCID 15538712 | 83.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06365612B2 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-cb73701bb7524c129e9fef26afd4297e |
| Source note | uspto-grants-2002_04 |