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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462004Generated: October 26, 2026

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

https://huagongshe.com/reaction/462004

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 II. 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 mixture 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 crystallized 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 numberUS04064258
Source datasetuspto-grants-1977_12
ORD IDord-31e0a5f61d7646c196df002360634e42
Source noteuspto-grants-1977_12