HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylpiperazine → HCID 21455926, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 21455917 | HCID 21455917 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 21455926 | HCID 21455926 | — |
Reaction Steps
In a manner analogous to that described in Example 21, 4.22 g. crude 3-(5-nitro-1-β-acetoxyethyl-2-imidazolyl)-6-chloro-s-triazolo[4,3-b]pyridazine were reacted with 4 g. 4-methylpiperazine in 20 ml. dioxan; after evaporation of the reaction mixture, the residue remaining behind was repeatedly digested with petroleum ether and then recrystallized from 15 ml. isopropanol, left to stand overnight and the crystals then filtered off with suction and washed with water. There were thus obtained 2.4 g. 3-(5-nitro- 1-β-acetoxyethyl-2-imidazolyl)-6-(4-methyl-1-piperazinyl)-s-triazolo[4,3-b]pyridazine, which has a melting point of 168° - 170° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03989832 |
| Source dataset | uspto-grants-1976_11 |
| ORD ID | ord-049c4638c07246e88db35f64445862ad |
| Source note | uspto-grants-1976_11 |