HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 1-t-Butylamino-3-[5-(2-[adamant-1-yl]ethylaminocarbonyl)thiazol-2-yloxy]-propan-2-ol maleate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | Maleate(2-) | HCID 5288227 | — |
| Reactant | 1-t-Butylamino-3-[5-(2-[adamant-1-yl]ethylaminocarbonyl)thiazol-2-yloxy]-propan-2-ol | HCID 21391917 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-t-Butylamino-3-[5-(2-[adamant-1-yl]ethylaminocarbonyl)thiazol-2-yloxy]-propan-2-ol maleate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04064258 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-31e0a5f61d7646c196df002360634e42 |
| Source note | uspto-grants-1977_12 |