Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Triethylamine hydrochloride | HCID 11130 | — |
| Reactant | 2-Morpholinoethylamine | HCID 408285 | — |
| Reactant | HCID 18998329 | HCID 18998329 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 18998380 | HCID 18998380 | — |
Reaction Steps
To a suspension of 5.40 g (0.02 mole) of 2-(dimethylamino)-5-chloro-7,8-dihydro-9H-thiopyrano[3,2-d]-1,2,4-triazolo[1,5-a]pyrimidine in 20 ml of 2-propanol 2,125 g (0.021 mole) of triethylamine and 2.73 g (0.021 mole) of 2-aminoethylmorpholine are successively added, and the reaction mixture is boiled for one hour. Upon cooling triethylamine hydrochloride gets separated, which is filtered and washed with 2-propanol. The filtrate is evaporated to dryness in vacuo and the residue is dissolved in chloroform. The solution thus obtained is extracted twice with water, dried over anhydrous Na2SO4 and evaporated in vacuo. The oily product is suspended in ethyl acetate, the crystalline product thus obtained is filtered off and washed with ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05478825 |
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| Source dataset | uspto-grants-1995_12 |
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| ORD ID | ord-bad2392ba57a4117af7ac89f50d16c08 |
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| Source note | uspto-grants-1995_12 |
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