HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (4S,5R)-N-(t-butylaminocarbonyl)-2-(2,4dimethoxyphenyl)-4phenyl-5-oxazolidine-carboxylic acid potassium salt
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (4S,5R)-N-(t-Butylaminocarbonyl)-2-(2,4-dimethoxyphenyl)-4-phenyl-5-oxazolidinecarboxylic acid methyl ester | HCID 53753692 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (4S,5R)-N-(t-butylaminocarbonyl)-2-(2,4dimethoxyphenyl)-4phenyl-5-oxazolidine-carboxylic acid potassium salt | HCID 69748715 | — |
Reaction Steps
A 100 mg (0.23 mM) quantity the less polar isomer of (4S,5R)-N-(t-butylaminocarbonyl)-2-(2,4-dimethoxyphenyl)-4-phenyl-5-oxazolidinecarboxylic acid methyl ester (Preparation 57, 5Ka) is stirred at room temperature under nitrogen in 3 mL MeOH. To this is added 0.1 mL water and 43 mg (0.31 mM) potassium carbonate. After 1 hour, TLC shows no starting material left. Store in freezer overnight. The next morning the solvent is evaporated to give (4S,5R)-N-(t-butylaminocarbonyl)-2-(2,4-dimethoxyphenyl)-4-phenyl-5-oxazolidinecarboxylic acid potassium salt (6Ka).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06911549B1 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-7820c651186349ca8e021727393a8314 |
| Source note | uspto-grants-2005_06 |