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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855493Generated: November 3, 2026

Methanol → HCID 57829738, compound

https://huagongshe.com/reaction/1855493

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBiphenylHCID 7095—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 13399964HCID 13399964—
Reactant4-Benzyl-2-chloro-6-methyl-pyrimidineHCID 86633618—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,4-DioxaneHCID 31275—
SolventDimethylacetamideHCID 31374—
ProductHCID 57829738HCID 57829738131.8%

Reaction Steps

A mixture of 4-benzyl-2-chloro-6-methyl-pyrimidine (104 mg, 0.48 mmol), 1-(4-amino-phenyl)-1H-imidazol-2-yl]-methanol (90 mg, 0.48 mmol) and potassium carbonate (1.33 g, 9.5 mmol) in dioxane (4 mL) and N,N-dimethylacetamide (1 mL) was degassed with nitrogen. Palladium(II) acetate (4.3 mg, 0.019 mmol) and 2-dicyclohexylphosphino)bi-phenyl (13.6 mg, 0.038 mmol) were added and the reaction mixture was irradiated in a microwave oven at 200° C. for 30 minutes. [1-(4-Amino-phenyl)-1H-imidazol-4-yl]-methanol (43 mg, 0.19 mmol) was added and the reaction mixture was irradiated in a microwave oven at 200° C. for another 25 minutes. The reaction mixture was filtered; the filtrate was diluted with ethyl acetate, washed with water and brine, dried with magnesium sulfate and concentrated in vacuo. Purification by column chromatography on silica eluting with dichloromethane/methanol (14:1 v/v) afforded the title compound as a light yellow solid (93 mg, 52%). MS ISP (m/e): 372.2 [(M+H)+]. Mp 95-98° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962834B2
Source datasetuspto-grants-2015_02
ORD IDord-e4efc3a95f2d4029a7e45f3752f7a8d8
Source noteuspto-grants-2015_02