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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 59716637HCID 59716637—
SolventPyridineHCID 1049—
ProductHCID 59716612HCID 5971661278%

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378418B2
Source datasetuspto-grants-2008_05
ORD IDord-1daecfd8ecdc43c38747d49c505133c3
Source noteuspto-grants-2008_05