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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855419Generated: October 30, 2026

2-(Dicyclohexylphosphino)biphenyl → HCID 57829762, compound

https://huagongshe.com/reaction/1855419

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Dicyclohexylphosphino)biphenylHCID 2734216—
Reactant3-methoxy-4-(4-methyl-1H-imidazol-1-yl)anilineHCID 45480181—
ReactantHCID 62476925HCID 62476925—
ReactantHCID 86633621HCID 86633621—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 57829762HCID 5782976237%

Reaction Conditions

Temperature200 °C

Reaction Steps

Palladium acetate (7.1 mg, 0.03 mmol) and 2-(dicyclohexylphosphino)biphenyl (23.1 mg, 0.64 mmol) were dissolved in dioxane (3.6 mL) and stirred for 10 minutes at. Sodium tert.-butylate (59 mg, 0.6 mmol), 3-methoxy-4-(4-methyl-imidazol-1-yl)-phenylamine (81 mg, 0.4 mmol) and 1:1 mixture of 2-chloro-4-cyclopentyloxy-6-methyl-pyrimidine and 4-chloro-2-cyclopentyloxy-6-methyl-pyrimidine (94 mg, 0.44 mmol) were added and the reaction was heated to 200° C. for 30 minutes in a microwave oven. The solvent was evaporated under reduced pressure and the residue was taken up in water and extracted twice with ethyl acetate. The combined organic layers were washed with brine, dried over sodium sulfate, filtered and evaporated under reduced pressure to dryness. The residue was purified by column chromatography on silica gel using methylenechloride/methanol (19:1 v/v) as eluent to yield the title compound as a white solid (56 mg, 37%). MS ISP (m/e): 380.1 (100) [(M+H)+]. 1H NMR (CDCl3, 300 MHz): δ (ppm)=7.70 (s, 1H), 7.62 (s, 1H), 7.15 (d, 1H), 7.07 (d, 1H), 7.05 (s, 1H), 6.87 (s, 1H), 6.06 (s, 1H), 5.30 (m, 1H), 3.85 (s, 3H), 2.33 (s, 3H), 2.30 (s, 3H), 1.75-2.00 (m, 6H), 1.60-1.68 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962834B2
Source datasetuspto-grants-2015_02
ORD IDord-05a656810a1246b2b69d4a078827759a
Source noteuspto-grants-2015_02