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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369011Generated: November 2, 2026

Dichloromethane → HCID 66584551, compound

https://huagongshe.com/reaction/2369011

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 66584820HCID 66584820—
ReactantHCID 178505454HCID 178505454—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 66584551HCID 6658455160%

Reaction Conditions

Temperature100 °C

Reaction Steps

To 3-iodo-5-(1-(tetrahydro-2H-pyran-4-ylamino)ethyl)-N,N-bis((2-(trimethylsilyl)ethoxy)methyl)pyrazolo[1,5-a]pyrimidin-7-amine (0.14 g, 0.21 mmol) was added 6-fluoroquinoline boronate (0.11 g, 0.42 mmol), K2CO3 (87 mg, 0.63 mmol), PdCl2(dppf).CH2Cl2 (18 mg, 0.02 mmol), dioxane (4 ml) and H2O (1 ml). The resulting mixture was heated at 100° C. for 2 hours, at which time LC/MS analysis confirmed full consumption of starting material. On cooling, the solvent was rotoevaporated, and the crude was redissolved in DCM (40 ml), washed with water (1×5 ml), brine (1×5 ml), dried over MgSO4. Solvent was removed in vacuo and the residue was purified by column chromatography on silica gel. Elution with MeOH/EtOAC (0-20%) gave desired product, 3-(6-fluoroquinolin-3-yl)-5-(1-(tetrahydro-2H-pyran-4-ylamino)ethyl)-N,N-bis((2-(trimethylsilyl)ethoxy)methyl)pyrazolo[1,5-a]pyrimidin-7-amine (84 mg, 60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703784B2
Source datasetuspto-grants-2014_04
ORD IDord-5c29257c6e0f4182bb295cc2339ccf6f
Source noteuspto-grants-2014_04