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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372189Generated: October 29, 2026

Morpholine → N-morpholino-3-(5-4'-methylhexylaminocarbonylthiazol-2-oxy)-2-propanol

https://huagongshe.com/reaction/372189

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantN-(4-Methylhexyl)-2-[(oxiran-2-yl)methoxy]-1,3-thiazole-5-carboxamideHCID 20328376—
Reactant1,2-Epoxy-3-(5-aminocarbonylthiazol-2-oxy)-propaneHCID 20328399—
SolventEthanolHCID 702—
ProductN-morpholino-3-(5-4'-methylhexylaminocarbonylthiazol-2-oxy)-2-propanolHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04089865
Source datasetuspto-grants-1978_05
ORD IDord-c7ed3538e3fa47ba8c6616ce3b2f164a
Source noteuspto-grants-1978_05