HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369190Generated: October 28, 2026
1H-1,2,4-Triazole → HCID 23284976, compound
https://huagongshe.com/reaction/369190
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1H-1,2,4-Triazole | HCID 9257 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 23285053 | HCID 23285053 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 23284976 | HCID 23284976 | 15.1% |
Reaction Steps
1.16 g of 1,2,4-triazole and 1.16 g of potassium carbonate were added to a solution of 2.00 g of 4-[N-methyl-N-(2-phenylethyl)amino]-1-(6-chloronicotinoyl)piperidine in 10 ml of dimethyl sulfoxide. The container inside was purged with nitrogen and the container contents were stirred at 100° C. for 4 hours. The reaction mixture was cooled and water was added thereto. The mixture was extracted with ethyl acetate. The extract was washed with a saturated aqueous sodium chloride solution, dried with anhydrous magnesium sulfate, and concentrated. The residue was purified by a silica gel column chromatography (eluant: methylene chloride/methanol=150/1). The product was subjected to crystallization from diethyl ether and then to recrystallization from ethyl acetate-diethyl ether to obtain 0.33 g of 4-[N-methyl-N-(2-phenylethyl)amino]-1-[6-(1,2,4-triazol-1-yl)nicotinoyl]piperidine as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06136826 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-d1c7aa17f129405fb94f5904bba3b5fa |
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| Source note | uspto-grants-2000_10 |
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