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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098820Generated: November 2, 2026

(3-Acetamidophenyl)boronic acid → HCID 59592900, compound

https://huagongshe.com/reaction/2098820

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Acetamidophenyl)boronic acidHCID 157274—
Reactant4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazoleHCID 45480186—
Reactant2-Chloro-6-iodo-7-methyl-4-morpholinothieno[3,2-d]pyrimidineHCID 59592880—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
SolventSodium CarbonateHCID 10340—
ProductHCID 59592900HCID 59592900—

Reaction Conditions

Temperature150 °C

Reaction Steps

2-Chloro-6-iodo-7-methyl-4-morpholinothieno[3,2-d]pyrimidine from Example 12 (0.1 g, 0.3 mmol), 3-Acetamidobenzeneboronic acid (50 mg, 0.3 mmol), and bis(triphenylphosphine)palladium(II) dichloride (9 mg, 13 μmmol) in 1 M aqueous Na2CO3 (0.5 mL) and acetonitrile (0.5 mL) were heated to 100° C. in a sealed microwave reactor for 10 min. Upon completion, 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole 7 (122 mg, 0.5 mmol), bis(triphenylphosphine)palladium(II) dichloride (9 mg, 13 μmol), 1 M aqueous Na2CO3 (1 mL), and acetonitrile (1 mL) 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 359 after reverse phase HPLC purification (10 mg). MS (Q1) 485 (M)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450315B2
Source datasetuspto-grants-2013_05
ORD IDord-186f544997b144319678905260150835
Source noteuspto-grants-2013_05