HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224261Generated: October 29, 2026
Hydrazine hydrate (1:1) → HCID 59716612, compound
https://huagongshe.com/reaction/2224261
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 59716637 | HCID 59716637 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 59716612 | HCID 59716612 | 78% |
Reaction Steps
To a solution of 3-chloro-5-(4-fluorophenyl)4-(pyridin-4-yl)pyridazine (586 mg, 2.05 mmol) in pyridine (3 mL) at RT was added hydrazine monohydrate (0.6 mL). After addition, the reaction was heated to 100° C. for 3 h. After this time, the reaction mixture was cooled to RT. The reaction mixture was concentrated under reduced pressure and the residue was diluted with water. The resulting mixture was then extracted with EtOAc (3×50 mL). The combined organic layers were washed with saturted Nacl. The organic layer was dried (Na2SO4), filtered and concentrated. The resulting residue was triturated with EtOAc-hexane to give the title compound, 1-(5-(4-fluorophenyl)4-(pyridin-4-yl)pyridazin-3-yl)hydrazine (450 mg, 78%) as an off-white solid. LC/MS (method A): RT=1.10 min, (M+H)+=282.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07378418B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-1daecfd8ecdc43c38747d49c505133c3 |
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| Source note | uspto-grants-2008_05 |
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