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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046502Generated: November 1, 2026

Acetonitrile → 1-Morpholino(4-(4-(tetrahydro-2H-pyran-4-yloxy)-1-trityl-1H-pyrazolo[4,3-c]pyridin-3-yl)phenyl)methanone

https://huagongshe.com/reaction/1046502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPotassium AcetateHCID 517044—
Reactant[4-(Morpholine-4-carbonyl)phenyl]boronic acidHCID 2773546—
ReactantHCID 66826813HCID 66826813—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
Product1-Morpholino(4-(4-(tetrahydro-2H-pyran-4-yloxy)-1-trityl-1H-pyrazolo[4,3-c]pyridin-3-yl)phenyl)methanoneHCID 66828967—

Reaction Conditions

Temperature150 °C

Reaction Steps

3-iodo-4-(tetrahydro-2H-pyran-4-yloxy)-1-trityl-1H-pyrazolo[4,3-c]pyridine (100 mg, 0.170 mmol), 4-(morpholine-4-carbonyl)phenylboronic acid (48 mg, 0.204 mmol), and 1,1′-bis(diphenylphosphino)ferrocenepalladium chloride (13.9 mg, 0.017 mmol) were charged in a microwave vial equipped with a stir bar. Acetonitrile (1.0 mL) and 1.0 M potassium acetate in water (0.41 mL) were then added, the reaction mixture was degassed with nitrogen for 5 min and then heated to 150° C. under microwave irradiation for 40 min. The crude mixture was filtered through Celite®, and concentrated to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569281B2
Source datasetuspto-grants-2013_10
ORD IDord-6210529ed0b3448ab6cc90d77be35921
Source noteuspto-grants-2013_10