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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027498Generated: October 30, 2026

Water → HCID 58382520, compound

https://huagongshe.com/reaction/1027498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-Aminophenylboronic acidHCID 92269—
ReactantTris(furan-2-yl)phosphaneHCID 521585—
ReactantHCID 67176736HCID 67176736—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
CatalystCuprous 2-thiophenecarboxylateHCID 11194830—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 58382520HCID 5838252031.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

Under argon atmosphere, 13.1 mg of tris(dibenzylideneacetone)dipalladium and 13.3 mg of tri(furan-2-yl)phosphine were added to a solution of 125 mg of 5-(4-chloro-benzyl)-2-methylsulfanyl-7-propoxy-oxazolo[5,4-d]pyrimidine, 81.7 mg of copper(I)thiophene-2-carboxylate and 58.7 mg of 3-amino-benzeneboronic acid in 3.5 ml of tetrahydrofuran. The mixture was heated to 80° C. for 2 h in a microwave reactor (CEM Discover). After cooling, 3 ml of water and 3 ml of ethyl acetate were added. The mixture was filtered through a ChemElut cartridge and the cartridge washed with ethyl acetate. The combined filtrates were evaporated in vacuo. Preparative HPLC (method HPLC1) of the residue yielded 44 mg of the title compound in the form of the 3-[5-(4-chloro-benzyl)-7-propoxy-oxazolo[5,4-d]pyrimidin-2-yl]-phenylamine trifluoroacetic acid salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735387B2
Source datasetuspto-grants-2014_05
ORD IDord-68cfa3a0d69a42da8a4ec561f71d8c5d
Source noteuspto-grants-2014_05