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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891428Generated: October 30, 2026

Isopropanol → (R)-2-(3,4-Difluorophenyl)-4-[3-(tert-butyldimethylsiloxy)-1-butoxy]-5-[4-(methylthio)phenyl]-3(2H)-pyridazinone

https://huagongshe.com/reaction/891428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant4-(Methylthio)phenylboronic acidHCID 2733959—
Reactant(R)-2-(3,4-Difluorophenyl)-4-[3-(tert-butyldimethylsiloxy)-1-butoxy]-5-bromo-3(2H)-pyridazinoneHCID 23598336—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
Product(R)-2-(3,4-Difluorophenyl)-4-[3-(tert-butyldimethylsiloxy)-1-butoxy]-5-[4-(methylthio)phenyl]-3(2H)-pyridazinoneHCID 68948236—

Reaction Conditions

Temperature70 °C

Reaction Steps

Under a nitrogen atmosphere, a mixture of the product from Example 545C (0.98 g, 2 mmol), 4-(methylthio)benzeneboronic acid (0.4 g, 2.4 mmol), K3PO4 (1.2 g, 6 mmol), PdCl2(PPh3)2 (28 mg, 0.04 mmol), isopropanol (9 mL), and water (1 mL) was stirred at 70° C. for 4 hours. The reaction mixture was then cooled to room temperature, water (30 mL) was added and stirring was continued for 2 hours. The crude black precipitate was collected by filtration then Washed with water (10 mL) and hexane (10 mL). This title intermediate was used without further purification in the following oxidation/deprotection step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001895B2
Source datasetuspto-grants-2006_02
ORD IDord-dab3acf4c7d942c1abaeef394f09eff1
Source noteuspto-grants-2006_02