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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | 1,2-Epoxy-3-[5-(hex-5-enylaminocarbonyl)thiazol-2-yloxy]propane | HCID 21392728 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-t-Butylamino-3-[5-(hex-5-enylaminocarbonyl)thiazol-2-yloxy]propan-2-ol | HCID 21391899 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04064259 |
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| Source dataset | uspto-grants-1977_12 |
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| ORD ID | ord-c37e19a8066c430eb6c99464db9a5d5b |
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| Source note | uspto-grants-1977_12 |
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