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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098868Generated: November 2, 2026

Phenylboronic Acid → HCID 24969129, compound

https://huagongshe.com/reaction/2098868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylboronic AcidHCID 66827—
Reactant5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo(2,3-b)pyridineHCID 24208789—
Reactant2-Chloro-6-iodo-7-methyl-4-morpholinothieno[3,2-d]pyrimidineHCID 59592880—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
SolventSodium CarbonateHCID 10340—
ProductHCID 24969129HCID 24969129—

Reaction Conditions

Temperature150 °C

Reaction Steps

2-Chloro-6-iodo-7-methyl-4-morpholinothieno[3,2-d]pyrimidine from Example 12 (0.2 g, 0.5 mmol), phenylboronic acid (60 mg, 0.5 mmol), and bis(triphenylphosphine)palladium(II) dichloride (18 mg, 25 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 (180 mg, 0.75 mmol) and bis(triphenylphosphine)palladium(II) dichloride (13 mg, 20 μmol) 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 420 after reverse phase HPLC purification (57 mg). MS (Q1) 428 (M)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450315B2
Source datasetuspto-grants-2013_05
ORD IDord-59b5bc47c46a4367a64f26efbe690858
Source noteuspto-grants-2013_05