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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556403Generated: October 25, 2026

Ethyl Acetate → 7-(4-n-Butoxy-phenyl)-4-ethoxy-9-methyl-2-piperazin-1-yl-thieno[2,3-d:4,5-d']dipyrimidine

https://huagongshe.com/reaction/556403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantCesium carbonateHCID 10796—
Reactant4-ButoxyphenolHCID 31233—
Reactant7-(4-Bromophenyl)-4-ethoxy-9-methyl-2-piperazin-1-yl-thieno[2,3-d:4,5-d']dipyrimidineHCID 59755063—
SolventTolueneHCID 1140—
Product7-(4-n-Butoxy-phenyl)-4-ethoxy-9-methyl-2-piperazin-1-yl-thieno[2,3-d:4,5-d']dipyrimidineHCID 66991918—

Reaction Conditions

Temperature180 °C

Reaction Steps

100 mg (0.21 mmol) 7-(4-bromophenyl)-4-ethoxy-9-methyl-2-piperazin-1-yl-thieno[2,3-d:4,5-d′]dipyrimidine, 51 mg (0.31 mmol) 4-n-butoxyphenol, 134 mg (0.41 mmol) Cs2CO3, 1 μl (5 mole %) ethyl acetate and 1.5 mg (5 mole %) CuBr were suspended in 5 ml absolute toluene and heated in a microwave oven at 180° C. for 17 h. Thereafter, the solvent was removed and the residue was purified by means of flash chromatography. 4 mg (3%) of the title substance is obtained. ESI-MS [m/z]: 571

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058285B2
Source datasetuspto-grants-2011_11
ORD IDord-884943c3187e4723b65f9f125527d23f
Source noteuspto-grants-2011_11