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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461692Generated: October 25, 2026

Ethanol → 1-t-Butylamino-3-[5-(2-[adamant-1-yl]ethylaminocarbonyl)thiazol-2-yloxy]-propan-2-ol maleate

https://huagongshe.com/reaction/461692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantMaleic AcidHCID 444266—
ReactantMaleate(2-)HCID 5288227—
Reactant1-t-Butylamino-3-[5-(2-[adamant-1-yl]ethylaminocarbonyl)thiazol-2-yloxy]-propan-2-olHCID 21391917—
SolventDiethyl EtherHCID 3283—
Product1-t-Butylamino-3-[5-(2-[adamant-1-yl]ethylaminocarbonyl)thiazol-2-yloxy]-propan-2-ol maleateHCID 68119553—

Reaction Steps

This example illustrates methods of preparing the maleate addition salts of compounds of formula C. In this example one gram of 1-t-butylamino-3-[5-(2-[adamant-1-yl]ethylaminocarbonyl)thiazol-2-yloxy]-propan-2-ol is dissolved in a solution of 5 ml. of ethyl ether and 5 ml. of ethanol at 20° C. To this solution is added 10 ml. of a saturated solution of maleic acid in ethyl ether. The mixtutre is allowed to stand for one hour at room temperature. The resulting precipitate is recovered by filtration, washed three times with ethyl ether and then crystalized from a mixture of ethyl ether and ethanol (1:1) affording crystalline 1-t-butylamino-3-[5-(2-[adamant-1-yl]ethylaminocarbonyl)thiazol-2-yloxy]-propan-2-ol maleate, m.p. 180°-181° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04064135
Source datasetuspto-grants-1977_12
ORD IDord-4e99e4adbe9446e9b027cac08b511d3f
Source noteuspto-grants-1977_12