HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 23057961, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Chloro-6-hydrazinopyridazine | HCID 100787 | — |
| Reactant | 3-Cyanobenzoyl chloride | HCID 308483 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23057961 | HCID 23057961 | — |
Reaction Steps
To a solution of (6-chloropyridazin-3-yl)hydrazine and triethylamine in THF, 3-cyanobenzoyl chloride was added with cooling in ice, and stirred at room temperature for 1 hour. The reaction solution was combined with water, and the precipitate was collected by filtration, washed with water and diethyl ether to obtain, N′-(6-chloropyridazin-3-yl) -3-cytanobenzohydrazide. To this, acetic acid was added, and the mixture was stirred at 110° C. for 2 hours, the reaction solution was concentrated under reduced pressure, and the resultant crude crystal was washed with ethanol to obtain 3-(6-chloro-1,2,4-triazolo[4,3-b]pyridazin-3-yl)benzonitrile. Dat (F:256).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07173033B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-1c7bc2b547664a238ea26b716c2e6dbd |
| Source note | uspto-grants-2007_02 |