HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloroethyl methyl ether → N-[[(5S)-3-[3-fluoro-4-(2-methoxyethylsulfanyl)phenyl]-2-oxo-oxazolidin-5-yl]methyl]acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloroethyl methyl ether | HCID 12316 | — |
| Reactant | 5-(S)-Acetamidomethyl-3-[4'-triphenylmethylthio-3'-fluorophenyl]oxazolidine-2-one | HCID 22966197 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | N-[[(5S)-3-[3-fluoro-4-(2-methoxyethylsulfanyl)phenyl]-2-oxo-oxazolidin-5-yl]methyl]acetamide | HCID 485759 | — |
Reaction Steps
Prepared according to Method B of the General Procedures for Preparation of 5-(S)-(N-Acylaminomethyl)-3-[4′-(substituted)thio-3′-fluorophenyl]oxazoli-dine-2-ones from 5-(S)-acetamidomethyl-3-[4′-(triphenylmethyl)thio-3′-fluorophenyl]oxazolidine-2-one with 2-chloroethyl methyl ether (0.036 g, 0.38 mmol) in N-methylpyrrolidine-2-one (1 mL). The synthesis was performed at r.t. for 2 h. The crude product was purified by TLC (eluent: 10% methanol in dichloromethane). Yield 0.034 g (52%). MS (m/z): 343 [M+H]+. 1H NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06239152B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-ff6a05813f3f47be87935f4d9f94502f |
| Source note | uspto-grants-2001_05 |