HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 5-{4-[2-(5-Phenylthiomethyl-2-oxooxazolidin-3-yl)propoxy]benzyl}thiazolidine-2,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 5-{4-[2-(3-Phenylthio-2-hydroxypropylamino)propoxy]benzyl}thiazolidine-2,4-dione | HCID 21474787 | — |
| Product | 5-{4-[2-(5-Phenylthiomethyl-2-oxooxazolidin-3-yl)propoxy]benzyl}thiazolidine-2,4-dione | HCID 15383946 | — |
Reaction Steps
A procedure similar to that described in Example 4 was repeated, except that 1.2 g of 5-{4-[2-(3-phenylthio-2-hydroxypropylamino)propoxy]benzyl}thiazolidine-2,4-dione (prepared as described in Example 37), 0.52 g of N,N'-carbonyldiimidazole and 20 ml of anhydrous dimethylformamide were used, to give 1.15 g of the title compound as a 1:1 mixture of two kinds of diastereomers having an Rf value of 0.30 (polar) and an Rf value of 0.38 (less polar) (on silica gel thin layer chromatography, using a 1:1 by volume mixture of ethyl acetate and hexane as the developing solvent).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05688823 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-1b40918b7e224a16be6dc07f009b7487 |
| Source note | uspto-grants-1997_11 |