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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575996Generated: October 31, 2026

Potassium Carbonate → HCID 57488517, compound

https://huagongshe.com/reaction/575996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-Bis(diphenylphosphino)butaneHCID 82124—
Reactant[[(2,2-Dimethyl-3-butyn-1-yl)oxy]methyl]benzeneHCID 57488516—
ReactantHCID 57516852HCID 57516852—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetonitrileHCID 6342—
ProductHCID 57488517HCID 57488517—

Reaction Conditions

Temperature80 °C

Reaction Steps

Palladium acetate (0.01 eq), dppb (0.015 eq), CuI (0.015 eq) and potassium carbonate (3 eq) are suspended in acetonitrile (1.2 vol). After stirring for 15 minutes, a solution of 4-benzyloxy-3,3-dimethylbut-1-yne (1.1 eq) in acetonitrile (0.2 vol) is added. The mixture is sparged with nitrogen gas for 1 h and then a solution of (R)-1-((4-amino-2-bromo-5-fluorophenyl)amino)-3-(benzyloxy)propan-2-ol free base (1 eq) in acetonitrile (4.1 vol) is added. The mixture is sparged with nitrogen gas for another hour and then is heated to 80° C. Reaction progress is monitored by HPLC and the reaction is usually complete within 3-5 h. The mixture is cooled to room temperature and then filtered through Celite. The cake is washed with acetonitrile (4 vol). The combined filtrates are azeotroped to dryness and then the mixture is polish filtered into the next reactor. The acetonitrile solution of (R)-1-((4-amino-2-(4-(benzyloxy)-3,3-dimethylbut-1-yn-1-yl)-5-fluorophenyl)amino)-3-(benzyloxy)propan-2-ol thus obtained is used directly in the next procedure (cyclization) without further manipulation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09035072B2
Source datasetuspto-grants-2015_05
ORD IDord-eb5e87aae2674f5fad7bd9e3ffc8017d
Source noteuspto-grants-2015_05