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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098867Generated: November 1, 2026

Phenylboronic Acid → HCID 59593176, compound

https://huagongshe.com/reaction/2098867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylboronic AcidHCID 66827—
Reactant5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo(2,3-b)pyridineHCID 24208789—
Reactant4-(2-Chloro-6-iodothieno[3,2-d]pyrimidin-4-yl)morpholineHCID 59593061—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
SolventSodium CarbonateHCID 10340—
ProductHCID 59593176HCID 59593176—

Reaction Conditions

Temperature150 °C

Reaction Steps

2-Chloro-6-iodo-4-morpholinothieno[3,2-d]pyrimidine 19 from Example 12 (0.2 g, 0.6 mmol), phenylboronic acid (70 mg, 0.6 mmol), and bis(triphenylphosphine)palladium(II) dichloride (20 mg, 30 μmol) in 1 M aqueous Na2CO3 (1 mL) and acetonitrile (1 mL) were heated to 100° C. in a sealed microwave reactor for 10 min. Upon completion, 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine (210 mg, 0.87 mmol) and bis(triphenylphosphine)palladium(II) dichloride (20 mg, 30 mop were added and the mixture was heated to 150° C. in a sealed microwave reactor for 20 min. The mixture was extracted with EtOAc and CH2Cl2. The combined organics were concentrated to yield 419 after reverse phase HPLC purification (45 mg). MS (Q1) 414 (M)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450315B2
Source datasetuspto-grants-2013_05
ORD IDord-0710fd5e81f14e67bebd21db6275b43c
Source noteuspto-grants-2013_05