Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098850Generated: November 1, 2026

3-(Methylsulfonyl)phenylboronic acid → HCID 59592895, compound

https://huagongshe.com/reaction/2098850

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Methylsulfonyl)phenylboronic acidHCID 2773542—
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 59592895HCID 59592895—

Reaction Conditions

Temperature150 °C

Reaction Steps

2-Chloro-6-iodo-7-methyl-4-morpholinothieno[3,2-d]pyrimidine from Example 12 (0.3 g, 0.8 mmol), 3-(methylsulfonyl)phenylboronic acid (0.3 g, 1.5 mmol), and bis(triphenylphosphine)palladium(II) dichloride (30 mg, 40 μmmol) in 1 M aqueous Na2CO3 (1.5 mL) and acetonitrile (1.5 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 (0.4 g, 1.7 mmol), and bis(triphenylphosphine)palladium(II) dichloride (30 mg, 40 μmol) were added into the same pot. The reaction 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 395 after reverse phase HPLC purification (82 mg). MS (Q1) 506 (M)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450315B2
Source datasetuspto-grants-2013_05
ORD IDord-98a3c8e7be8448c381a2e84280bc9e2c
Source noteuspto-grants-2013_05