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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422476Generated: October 30, 2026

Potassium Carbonate → Lhd-221

https://huagongshe.com/reaction/1422476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(1-Benzothiophen-3-yl)boronic acidHCID 2776344—
Reactant4-(2-((2-Chloro-9-isopropyl-9H-purin-6-yl)amino)ethyl)phenolHCID 75529970—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
ProductLhd-221HCID 46199207—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 4-(2-(2-chloro-9-isopropyl-9H-purin-6-ylamino)ethyl)phenol (950 g), thianaphthene-3-boronic acid (561 g), dichlorobis(triphenylphosphine)palladium(II) (10.1 g), potassium carbonate (791 g), water (3.25 L), and DMA (3.25 L) was stirred under a nitrogen atmosphere for 10 min. The stirred mixture was then heated at 70° C. for 14 h. Ethyl acetate (6.5 L) and water (3.25 L) were added, and the mixture was filtered through Celite (125 g) at 50° C., rinsing with ethyl acetate (1.0 L). The layers were separated, and the aqueous layer was extracted at 50° C. with additional ethyl acetate (7.5 L). The combined organic layers were washed with water (3×2.5 L), then distilled to remove about 2.5 L of solvent. Tetrahydrofuran (2.5 L) and silica bond thio silica gel (200 g) were added. The mixture was stirred at 70° C. for 16 hr, then was filtered, washing the pad with ethyl acetate (1.0 L). The combined filtrates were concentrated at atmospheric pressure to a volume of about 5 L, then the mixture was allowed to cool. The resulting solid was collected and washed with ethyl acetate (2×1.0 L) to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927281B2
Source datasetuspto-grants-2015_01
ORD IDord-05e8929f59434d45b41ca9f328a3614b
Source noteuspto-grants-2015_01