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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 965873Generated: October 30, 2026

Triphenylphosphine → HCID 10192636, compound

https://huagongshe.com/reaction/965873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant4-Amino-2-bromopyridineHCID 346455—
ReactantHCID 4372073HCID 4372073—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
ProductHCID 10192636HCID 1019263639.2%

Reaction Steps

Under inert atmosphere (Ar) a mixture of palladium-(II)-acetate (0.117 mg, 0.5 mmol) and triphenylphosphine (0.248 g, 0.9 mmol) in DMF (13 ml) was stirred for 30 min at rt. 2-Bromo-pyridin-4-ylamine (0.90 g, 5.2 mmol) (H. J. den Hertog, C. R. Kolder and W. P. Combe, Rec. Trav. Chim., 1951, 70, 591) was added followed by tributyl-styryl-stannane (3.93 g, 10 mmol). After heating at 130° C. for 15 min the solvent was evaporated and the residue partitioned between AcOEt and 3N HCl. The aqueous phase was neutralized with 6N NaOH and extracted with AcOEt. The organic phase was dried with Na2SO4, concentrated and chromatographed (SiO2 with CH2Cl2/CH3OH/NH4OH=140/10/1) to give the title compound (0.40 g, 39%) as a colorless solid. Mp. 164-165° C. (AcOEt), MS: 196 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06951875B2
Source datasetuspto-grants-2005_10
ORD IDord-f352c803ac0148e8a4b27bb1a3f6a67e
Source noteuspto-grants-2005_10