HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1854808Generated: November 1, 2026
Piperazine → 3-(Piperazin-1-yl)-1,2,4-triazine
https://huagongshe.com/reaction/1854808
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 3-(Methylsulfanyl)-1,2,4-triazine | HCID 321839 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 3-(Piperazin-1-yl)-1,2,4-triazine | HCID 12296696 | 69% |
Reaction Steps
3.45 g (40.1 mmoles) of piperazine is placed in the presence of 1.7 g (13.4 mmoles) of intermediate 2a in 1-butanol. 6.5 ml (47 mmoles) of triethylamine is added and the mixture is heated for 24 hours at 120° C. After concentrating the reaction medium, the residue obtained is taken up with ethyl acetate and washed with water. After drying on MgSC4, the organic phase is concentrated to dryness. The residue obtained is purified by flash chromatography (CH2Cl2-MeOH-NH4OH gradient: 100-0-0 to 90-9-1). 1.52 g of intermediate 5a is obtained in brown oil form (yield: 69%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08962837B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-b694cb8baa18405b9e6d17258255d1a4 |
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| Source note | uspto-grants-2015_02 |
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