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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098623Generated: October 31, 2026

3-Aminophenylboronic acid → HCID 59593132, compound

https://huagongshe.com/reaction/2098623

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 numberUS08450315B2
Source datasetuspto-grants-2013_05
ORD IDord-0792d526551c47cf8d705babfb9d7954
Source noteuspto-grants-2013_05