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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093214Generated: October 26, 2026

Hydrochloric Acid → HCID 25261557, compound

https://huagongshe.com/reaction/1093214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1H-Indol-2-ylboronic acidHCID 22567358—
Reactant3-(6-chloro-1-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-8-oxa-3-azabicyclo[3.2.1]octaneHCID 86629376—
CatalystHCID 178418397HCID 178418397—
SolventSodium CarbonateHCID 10340—
SolventToluene ethanolHCID 21863594—
ProductHCID 25261557HCID 25261557—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 3-(6-chloro-1-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-8-oxa-3-azabicyclo[3.2.1]octane (80 mg, 0.27 mmol), 5-indoylboronic acid (66 mg, 0.41 mmol), and tetrakis(triphenylphosphine)palladium(0) (35 mg, 10 mol %) in toluene/ethanol (1:1, 3 mL) and 2 M aqueous sodium carbonate solution (1 mL) was heated in a Smith process vial in the microwave reactor for one hour at 120° C. The cooled mixture was acidified with concentrated hydrochloric acid and then concentrated to dryness under reduced pressure. The crude residue was purified via reverse-phase high performance liquid chromatography using a Phenomenex Prodigy 21 mm×250 mm column to provide 1-ethyl-6-(1H-indol-5-yl)-4-(8-oxa-3-azabicyclo[3.2.1]oct-3-yl)-1H-pyrazolo[3,4-d]pyrimidine. MS (ES+): 375.2 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129371B2
Source datasetuspto-grants-2012_03
ORD IDord-ee7d283118cd470298de706ab91fda1a
Source noteuspto-grants-2012_03