HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → 1-Formyl 4-[5,6-bis(2-pyridinyl)-1,2,4-triazin-3-yl]-piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | Di-2-pyridylethanedione | HCID 68115 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 4-Formyl-piperazinecarboximidamide hydroiodide | HCID 13036366 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Formyl 4-[5,6-bis(2-pyridinyl)-1,2,4-triazin-3-yl]-piperazine | HCID 22418759 | — |
Reaction Steps
A mixture of 4-formyl-piperazinecarboximidamide hydroiodide (prepared according to U.S. Pat. No. 4,351,832) in ethanol (4 ml) and ethanolic sodium ethoxide (1.4N, 6.8 ml) is stirred for 15 min and then anhydrous hydrazine (0.32 g) in ethanol (3 ml) is added. The mixture is stirred an additional 15 min, then 2,2'-pyridil (2.12 g) is added. The mixture is stirred for 12 hours at 25° and concentrated. The residue is chromatographed on silica gel eluting with a methylene chloride/methanol mixture. The appropriate fractions are pooled and concentrated to give 1-formyl 4-[5,6-bis(2-pyridinyl)-1,2,4-triazin-3-yl]-piperazine. Hydrolysis of the formamide in the usual way (PREPARATION A-14) gives the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05268477 |
| Source dataset | uspto-grants-1993_12 |
| ORD ID | ord-d1d18e472a2c4069a974d2efe4664bb8 |
| Source note | uspto-grants-1993_12 |