HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → Sulfuric acid mono-{(R)-1-chloromethyl-2-[4-(3-oxo-morpholin-4-yl)-phenylamino]-ethyl}ester potassium salt
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(4-Aminophenyl)morpholin-3-one | HCID 11194854 | — |
| Reactant | (R)-4-chloromethyl-[1,3,2]dioxathiolane 2,2-dioxide | HCID 42625092 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Sulfuric acid mono-{(R)-1-chloromethyl-2-[4-(3-oxo-morpholin-4-yl)-phenylamino]-ethyl}ester potassium salt | HCID 131734365 | 126.1% |
Reaction Steps
Under an atmosphere of nitrogen to a solution of a 7.11 g of (R)-4-chloromethyl-[1,3,2]dioxathiolane 2,2-dioxide (MW=156.59; 1.38 eq.) in 95 mL of acetonitrile were added 6.34 g of 4-(4-aminophenyl)-morpholin-3-one (APMO) (MW=192.22; 1 eq.) and 3.29 g (MW=138.21; 0.72 eq.) of potassium carbonate. The reaction mixture was stirred for 24 h at room temperature. Then the resulting suspension was cooled to 0° C. After stirring for at least 2 h at this temperature, the product was isolated by filtration and the filter cake was washed with 50 mL of acetonitrile. After drying in vacuo at 30° C., 12.09 g of the crystalline title compound (MW=402.90) were isolated. Yield=91.0%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09221771B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-61610dc613b649acbb6e8f1fd3b6436d |
| Source note | uspto-grants-2015_12 |