HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264873Generated: October 30, 2026
Piperazine → 5-Amino-2-(2-furyl)-7-piperazinyl[1,2,4]triazolo[1,5-c]pyrimidine
https://huagongshe.com/reaction/1264873
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 5-Amino-7-chloro-2-(2-furyl)[1,2,4]triazolo[1,5-c]pyrimidine | HCID 9942767 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 5-Amino-2-(2-furyl)-7-piperazinyl[1,2,4]triazolo[1,5-c]pyrimidine | HCID 18613698 | 78% |
Reaction Steps
Into 180 mL of DMSO, 10.5 g (44.6 mmol) of Compound E and 19.2 g (223 mmol) of piperazine were dissolved, followed by stirring at 150° C. for about 2 hours. After completion of the reaction, the solvent was evaporated under reduced pressure, water was added to the residue, and the mixture was extracted with chloroform. The organic layer was washed with water and brine, and then dried over anhydrous magnesium sulfate. After evaporation of the solvent, the resulting residue was purified by silica gel column chromatography (23% aqueous ammonia/methanol/chloroform=1/10/90) and then recrystallized from ethyl acetate to obtain 9.91 g of Compound F as a white solid (yield: 78%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06545000B1 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-4ed4e073b107416ca31cf42e55bf4ca8 |
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| Source note | uspto-grants-2003_04 |
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