HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 5-{4-[2-(5-Benzyl-2-oxooxazolidin-3-yl)propoxy]benzyl}thiazolidine-2,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 5-{4-[2-(3-Phenyl-2-hydroxypropylamino)propoxy]benzyl}thiazolidine-2,4-dione | HCID 9801907 | — |
| Product | 5-{4-[2-(5-Benzyl-2-oxooxazolidin-3-yl)propoxy]benzyl}thiazolidine-2,4-dione | HCID 21474808 | — |
Reaction Steps
Following a procedure similar to that described in Example 4, 300 mg of 5-{4-[2-(3-phenyl-2-hydroxypropylamino)propoxy]benzyl}thiazolidine-2,4-dione (prepared as described in Example 7), 120 mg of N,N'-carbonyldiimidazole and 10 ml of anhydrous dimethylformamide were used. The resulting crude product was applied to a silica gel chromatography column, which was then eluted with a 3:2 by volume mixture of ethyl acetate and hexane, to give 200 mg of the title compound, melting at 60° C. to 70° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05688823 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-4e269d71d1a34d97bc296f57589abc56 |
| Source note | uspto-grants-1997_11 |