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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865824Generated: November 1, 2026

Water → HCID 178518926, compound

https://huagongshe.com/reaction/1865824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAcetonitrileHCID 6342—
Reactant3,6-Dichloro-4-(4-chlorophenyl)-5-(pyridin-4-yl)pyridazineHCID 59515531—
SolventDichloromethaneHCID 6344—
ProductHCID 178518926HCID 17851892648%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a round bottom flask was added 3,6-dichloro-4-(4-chlorophenyl)-5-(pyridin-4-yl)pyridazine (1.5 gm, 4.464 mmol), CH3CN (5 ml), water (1 ml) and LiOH monohydrate (0.938 gm, 22.32 mmol). The reaction was heated to 80° C. and stirred at this temperature for 4 hrs. After this time, the reaction was colled to rt and concentrated under reduced pressure. The residue was diluted with water (30 ml). The pH of the aqueous solution was adjusted to 7 with 1N HCl. The resulting solution was poured into a separatory funnel and extract with EtOAc (4×20 ml). The combined organic layers were washed with saturated aqueous NaCl (30 ml). The organic layer was then slurried with MgSO4 to remove excess water, filtered and concentrated to give a white solid residue. The residue was stirred in CH2Cl2 (10 ml) for 15 min. The solution was then filter and the solid was collected to give product 6-chloro-5-(4-chlorophenyl)-4-(pyridin-4-yl)pyridazin-3-ol as white solid (0.70 gm, 48% yield). HPLC retention time (method A) 1.332 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07629342B2
Source datasetuspto-grants-2009_12
ORD IDord-78b5ada592d5443c802e7d6b0117e62b
Source noteuspto-grants-2009_12