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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869151Generated: October 29, 2026

Triphenylarsine → HCID 86686127, compound

https://huagongshe.com/reaction/869151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylarsineHCID 11773—
Reactant6-Bromopyridine-3-carbonitrileHCID 5005718—
ReactantHexamethylditinHCID 6327618—
ReactantHCID 86686128HCID 86686128—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Solvent1,4-DioxaneHCID 31275—
SolventPotassium FluorideHCID 522689—
ProductHCID 86686127HCID 86686127—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a 20 dram vial was added 2-bromo-5-cyanopyridine (182 mg, 1.0 mmol, 1.0 equiv), hexamethylditin (639 mg, 1.1 mmol, 1.1 equiv), Cl2Pd(Ph3P)2 (91 mg, 0.13 mmol, 0.13 equiv), triphenylarsine (34 mg, 0.11 mmol, 0.11 equiv), and dioxane (7 mL). The reaction mixture was stirred and heated to 80° C. for 12 h. The reaction was then concentrated, followed by the addition of tert-butyl 6-bromopyridazin-3-yl(2-(4-fluorophenyl)-2-methylpropyl)carbamate (423 mg, 1.0 mmol, 1.0 equiv), Pd(Ph3P)4 (172 mg, 0.15 mmol, 0.15 equiv), and DMF (3.3 mL). The reaction was stirred and heated to 100° C. for 3 h. After cooling to room temperature, the reaction was diluted with aqueous potassium fluoride (5 mL), extracted with ethyl acetate (20 mL) and washed with brine (20 mL). The organic layer was then dried (Na2SO4), filtered, and concentrated to give crude tert-butyl 6-(5-cyanopyridin-2-yl)pyridazin-3-yl(2-(4-fluorophenyl)-2-methylpropyl)carbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969346B2
Source datasetuspto-grants-2015_03
ORD IDord-8d7815b732c442bca9dee9a9716380c1
Source noteuspto-grants-2015_03