HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224262Generated: October 31, 2026
1,1'-Carbonyldiimidazole → HCID 59716620, compound
https://huagongshe.com/reaction/2224262
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | HCID 59716612 | HCID 59716612 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59716620 | HCID 59716620 | 91.2% |
Reaction Steps
To a solution of 1,1′-carbonyldiimidazole (1.27 g, 7.86 mmol) in THF (20 mL) was added a suspension of 1-(5-(4-fluorophenyl)4-(pyridin-4-yl)pyridazin-3-yl)hydrazine (442 mg, 1.57 mmol) in THF (5 mL). After addition, the reaction mixture was heated to 66° C. After 20 min., the reaction mixture was cooled to RT and the reaction mixture was then concentrated under reduced pressure. The residue was diluted with water. The resultant mixture was extracted with EtOAc (3×100 mL). The combined organic layers were washed with saturated NaCl. The organic layer was dried (Na2SO4), filtered and concentrated. The resulting residue was triturated with EtOAc-hexane to give the title compound, 7-(4-fluorophenyl)-8-(pyridine-4-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3(2H)-one (440 mg, 91%) as a yellow solid. LC/MS (method A): RT=1.27 min, (M+H)+=308.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07378418B2 |
|---|
| Source dataset | uspto-grants-2008_05 |
|---|
| ORD ID | ord-7e961bd28456479597e5c561696cc1ed |
|---|
| Source note | uspto-grants-2008_05 |
|---|