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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2042236Generated: November 2, 2026

Potassium Carbonate → 2-chloro-N-(3,4,5-trimethoxyphenyl)thieno[3,2-d]pyrimidin-7-amine

https://huagongshe.com/reaction/2042236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3,4,5-TrimethoxyanilineHCID 32285—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Reactant7-Bromo-2-chlorothieno(3,2-d)pyrimidineHCID 56965724—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent(+-)-2-ButanolHCID 6568—
Product2-chloro-N-(3,4,5-trimethoxyphenyl)thieno[3,2-d]pyrimidin-7-amineHCID 8667322443%

Reaction Conditions

Temperature80 °C

Reaction Steps

7-Bromo-2-chlorothieno[3,2-d]pyrimidine (200 mg, 0.81 mmol) was dissolved in 2-butanol (4 mL) and then potassium carbonate (223 mg, 1.61 mmol) and 3,4,5-trimethoxybenzenamine (110 mg, 0.81 mmol) were added. After blowing nitrogen to the reaction mixture for 10 minutes, Pd2(dba)3 (50 mg, 0.048 mmol) and Xphos (35 mg, 0.073 mmol) were added. The reaction mixture was stirred at 80° C. for 2.5 hours and then filtered with celite. The filtrate was diluted with ethyl acetate and washed with brine. The organic layer was dried with magnesium sulfate, filtered with celite, and then concentrated. Purification by chromatography (15% ethyl acetate/hexane) yielded the target compound (120 mg, 43% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586580B2
Source datasetuspto-grants-2013_11
ORD IDord-7a752c1ca70b483eb182cc65ae1a475b
Source noteuspto-grants-2013_11