HuagongsheHuagongshe Chemistry Print Report · For research reference only
Morpholine → N-morpholino-3-(5-4'-methylhexylaminocarbonylthiazol-2-oxy)-2-propanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | N-(4-Methylhexyl)-2-[(oxiran-2-yl)methoxy]-1,3-thiazole-5-carboxamide | HCID 20328376 | — |
| Reactant | 1,2-Epoxy-3-(5-aminocarbonylthiazol-2-oxy)-propane | HCID 20328399 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-morpholino-3-(5-4'-methylhexylaminocarbonylthiazol-2-oxy)-2-propanol | HCID 131710592 | — |
Reaction Steps
This example illustrates further methods according to the invention of preparing the compounds of formula I to the invention. In this example 1 g. of morpholine is added to a solution containing 0.3 g. of 1,2-epoxy-3-(5-4'-methylhexylaminocarbonylthiazol-2-oxy)-propane in 20 ml. of anhydrous absolute ethanol at 20° C. The resulting mixture is monitored by thin-layer chromatographic analysis and allowed to stand until conversion of the 1,2-epoxy-3-(5-aminocarbonylthiazol-2-oxy)-propane is essentially complete. The mixture is then evaporated to dryness yielding a crude residue of 1 -(N-morpholino-3-(5-4'-methylhexylaminocarbonylthiazol-2-oxy)-2-propanol which is then further purified by thin-layer chromatography on silica gel.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04089865 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-c7ed3538e3fa47ba8c6616ce3b2f164a |
| Source note | uspto-grants-1978_05 |