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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461842Generated: October 31, 2026

Tert-Butylamine → 1-t-Butylamino-3-[5-(hex-5-enylaminocarbonyl)thiazol-2-yloxy]propan-2-ol

https://huagongshe.com/reaction/461842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButylamineHCID 6385—
Reactant1,2-Epoxy-3-[5-(hex-5-enylaminocarbonyl)thiazol-2-yloxy]propaneHCID 21392728—
SolventEthanolHCID 702—
Product1-t-Butylamino-3-[5-(hex-5-enylaminocarbonyl)thiazol-2-yloxy]propan-2-olHCID 21391899—

Reaction Conditions

Temperature-20 °C

Reaction Steps

This example illustrates method for preparing the compounds of the present invention. In this example a mixture containing 12 g. (0.037 mole) of 1,2-epoxy-3-[5-(hex-5-enylaminocarbonyl)thiazol-2-yloxy]propane, 12 g. (0.164 mole) of t-butylamine and 20 ml. of ethanol is allowed to stand at room temperature for 12 hours. The mixture is then evaporated under vacuum to remove the ethanol solvent and the resulting residue dissolved in 50 ml. of ethyl acetate and cooled to -20° C, and maintained at this temperature for two hours. The mixture is then filtered and the resulting filter cake washed with cold (about 0° C) ethyl ether and then recrystallized from ethyl acetate affording 1-t-butylamino-3-[5-(hex-5-enylaminocarbonyl)thiazol-2-yloxy]propan-2-ol, m.p. 80°-81° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04064259
Source datasetuspto-grants-1977_12
ORD IDord-c37e19a8066c430eb6c99464db9a5d5b
Source noteuspto-grants-1977_12