HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium → 6-chloro-2H,3H-[1,2,4]triazolo[4,3-b]pyridazin-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Ethyl 3-chloro-6-hydrazinylpyridazine-1(6H)-carboxylate | HCID 71390186 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-chloro-2H,3H-[1,2,4]triazolo[4,3-b]pyridazin-3-one | HCID 6407182 | — |
Reaction Steps
39 g. of 3-chloro-6-hydrazino-1(6H)pyridazinecarboxylic acid, ethyl ester (0.18 mol.) are added to a solution of 4.9 g. of sodium (0.216 mol.) in 400 ml. of absolute ethanol and the mixture is then refluxed for 4 hours with stirring. After cooling, the sodium salt of 6-chloro-1,2,4,-triazolo[4,3-b]pyridazin-3(2H)-one is filtered off, washed with ether and, after drying, dissolved in water. Acidification with acetic acid (25%) precipitates the free compound which then is filtered off, washed with water and dried, yielding 26 g. (85%) of 6-chloro-1,2,4-triazolo[4,3-b]pyridazin-3(2H)one, which is recrystallized from ethanol, m.p. 273°-274° .
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03994898 |
| Source dataset | uspto-grants-1976_11 |
| ORD ID | ord-470a46d588b1474fae5c020783146b1b |
| Source note | uspto-grants-1976_11 |