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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284820Generated: October 31, 2026

Dimethylformamide → HCID 117861350, compound

https://huagongshe.com/reaction/2284820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 90051817HCID 90051817—
ReactantHCID 90052291HCID 90052291—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
ProductHCID 117861350HCID 117861350—

Reaction Steps

To 3-((5-iodo-4-(methylamino)pyrimidin-2-yl)amino)benzonitrile (F219, 30 mg), tert-butyl ((S)-1-(((1S,3R)-3-ethynylcyclohexyl)amino)-1-oxopropan-2-yl)(methyl)carbamate (U2, 39.5 mg), bis(triphenylphosphine)palladium(II) dichloride (5.96 mg) and copper(I) iodide (3.24 mg), N,N-dimethylformamide (1 mL) and triethylamine (59 μL) were added at room temperature, and the mixture was stirred at the same temperature for 4 hours. To the reaction mixture, saturated aqueous sodium hydrogencarbonate and ethyl acetate were added. The organic layer was separated, washed successively with saturated aqueous ammonium chloride, water and saturated aqueous sodium chloride, and then dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent, 84 to 25% hexane in ethyl acetate) to obtain tert-butyl ((S)-1-(((1S,3R)-3-((2-((3-cyanophenyl)amino)-4-(methylamino)pyrimidin-5-yl)ethynyl)cyclohexyl)amino)-1-oxopropan-2-yl)(methyl)carbamate (U3, 27.4 mg) as pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145415B2
Source datasetuspto-grants-2015_09
ORD IDord-2ae8e240fa6947b793c2a3d0438909c2
Source noteuspto-grants-2015_09