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HRID 271424作成日:2026年10月25日

Ethyl Acetate → 1,3-dibenzyl-5,6-bis(4-chlorophenyl)pyrimidine-2,4(1H,3H)-dione

https://huagongshe.com/reaction/271424

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Sodium CarbonateHCID 10340—
反応物4-Chlorophenylboronic acidHCID 74299—
反応物1,3-dibenzyl-5-bromo-6-chloropyrimidine-2,4(1H,3H)-dioneHCID 59834797—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物1,3-dibenzyl-5,6-bis(4-chlorophenyl)pyrimidine-2,4(1H,3H)-dioneHCID 59834806—

反応手順

To a solution of 1,3-dibenzyl-5-bromo-6-chloropyrimidine-2,4(1H,3H)-dione (6.0 g, 14.8 mmol) in toluene (50 mL) at room temperature under argon was added 4-chlorophenylboronic acid (7.0 g, 44.77 mmol), tetrakis(triphenylphosphine)palladium (1.03 g, 0.89 mmol), and a solution of Na2CO3 (4.7 g, 44.34 mmol) in water (10 ml). The resulting suspension was stirred at reflux under argon for 6 h. After the reaction mixture was cooled to room temperature, water (50 mL) and EtOAc (75 mL) were added. The layers were separated. The organic layer was dried (MgSO4), filtered, and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography eluted 15% ethyl acetate-hexanes to obtain 7.2 g of the title compound as a white solid. HPLC/MS (MeOH-water with 10 mM NH4OAc): retention time=4.241 min, [M+H]30 =513.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07452892B2
出典データセットuspto-grants-2008_11
ORD IDord-3674e7106a52434baf203497da73df32
出典メモuspto-grants-2008_11