HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → (5R)-3-(3-Fluorophenyl)-5-[(4-methyl-1H-1,2,3-triazol-1-yl)methyl]-1,3-oxazolidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (5S)-5-(aminomethyl)-3-(3-fluorophenyl)-1,3-oxazolidin-2-one | HCID 11401559 | — |
| Reactant | N'-[2,2-dichloro-1-methylethylidene]-4-methylbenzenesulfonohydrazide | HCID 73181071 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (5R)-3-(3-Fluorophenyl)-5-[(4-methyl-1H-1,2,3-triazol-1-yl)methyl]-1,3-oxazolidin-2-one | HCID 58778317 | 70.2% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
N,N-Diisopropylethylamine (3.20 mL, 18.35 mM) was added to a solution of (5S)-5-(aminomethyl)-3-(3-fluorophenyl)-1,3-oxazolidin-2-one (0.77 g, 3.57 mM; see Dong Pharmaceuticals WO 0194342) in anhydrous methanol (25 mL). The solution was cooled to 0° C., and N′-[2,2-dichloro-1-methylethylidene]-4-methylbenzenesulfonohydrazide (1.28 g, 4.58 mM) was added. The solution was warmed to room temperature and stirred overnight. The reaction mixture was then concentrated under vacuum and chromatographed on silica gel using 2% methanol/dichloromethane to give 0.71 g of the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07396847B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-06845fd9ba70447abe3ec36d64e84578 |
| Source note | uspto-grants-2008_07 |