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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262043Generated: November 3, 2026

3-Aminophenylboronic acid → HCID 59593132, compound

https://huagongshe.com/reaction/2262043

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Aminophenylboronic acidHCID 92269—
Reactant4-(2-Chloro-6-iodothieno[3,2-d]pyrimidin-4-yl)morpholineHCID 59593061—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
SolventSodium CarbonateHCID 10340—
ProductHCID 59593132HCID 5959313299%

Reaction Steps

2-Chloro-6-iodo-4-morpholinothieno[3,2-d]pyrimidine 19 (300 mg), 3-aminophenylboronic acid (134 mg), and bis(triphenylphosphine)palladium(II) dichloride (55 mg) in 0.6 mL of 1M Na2CO3 aqueous solution and 0.6 mL of acetonitrile was heated to 100° C. in a sealed microwave reactor for 15 min. The reaction mixture was diluted with ethyl acetate (80 mL), washed with H2O (50 mL). The organic layer was dried over MgSO4, filtered and evaporated to yield 270 mg of 3-(2-chloro-4-morpholinothieno[3,2-d]pyrimidin-6-yl)benzenamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846929B2
Source datasetuspto-grants-2010_12
ORD IDord-3c81ee311f614dc9870aec11f97c5ea5
Source noteuspto-grants-2010_12