Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Ethyl 1-benzyl-3-oxopiperidine-4-carboxylate hydrochloride | HCID 2723880 | — |
| Reactant | 3-morpholin-4-yl-1H-1,2,4-triazol-5-amine | HCID 4417379 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178517719 | HCID 178517719 | 72% |
Reaction Steps
A mixture of 50.8 g (0.3 mole) of 5-amino-3-morpholino-1H-1,2,4-triazole, 89.3 g (0.3 mole) of 1-benzyl-4-carbethoxy-3-oxo-piperidine-hydrochloride and 220 ml of acetic acid is refluxed for 7 hours under stirring. The reaction mixture is allowed to stand overnight, the precipitate is filtered and washed with acetone. The product thus obtained is dissolved in a mixture of 400 ml of water and 100 ml of pyridine under heating to boiling for 15 minutes. The solution is allowed to stand for a day, the precipitated crystals are filtered and washed with acetone. The product thus obtained (83.9 g) is dissolved in 260 ml of hot pyridine, to the solution 1000 ml of acetone are added. The precipitated crystals are filtered and washed with acetone. Thus 78.9 g of the desired compound are obtained, yield 72%, m.p.: 315°-317° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04831029 |
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| Source dataset | uspto-grants-1989_05 |
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| ORD ID | ord-d442ff68ea8a4507bac7f54d43aa8b86 |
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| Source note | uspto-grants-1989_05 |
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