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HRID 1889396作成日:2026年10月25日

Triethylamine → 3-[2-(4-methoxyphenyl)-2-oxoethyl]-6-methylthieno[2,3-d]pyrimidine-2,4(1H,3H)-dione

https://huagongshe.com/reaction/1889396

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物TriphosgeneHCID 94429—
反応物Methyl-2-amino-5-methyl-3-thiophenecarboxylateHCID 675878—
反応物2-Amino-4'-methoxyacetophenone hydrochlorideHCID 12487188—
溶媒DichloromethaneHCID 6344—
生成物3-[2-(4-methoxyphenyl)-2-oxoethyl]-6-methylthieno[2,3-d]pyrimidine-2,4(1H,3H)-dioneHCID 59351590176.1%

反応手順

To a solution (100 mL) of methyl 2-amino-5-methylthiophene-3-carboxylate (2 g) in methylene chloride were added triphosgene (1.5 g) and triethylamine (4.24 mL), and the mixture was stirred at room temperature for 2 hr. To the reaction mixture were further added triethylamine (1.8 mL) and 2-amino-1-(4-methoxyphenyl)ethanone hydrochloride (2.6 g), and the mixture was further stirred at room temperature for 1 hr. The reaction mixture was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was dissolved in methanol (100 mL), sodium methoxide (3.16 g) was added, and the mixture was stirred at 60° C. for 2 hr. The reaction mixture was concentrated under reduced pressure, and the obtained residue was extracted with 1N hydrochloric acid and chloroform. The chloroform layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The precipitated solid was collected by filtration to give the title compound as a colorless solid (2.94 g, 76%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08501750B2
出典データセットuspto-grants-2013_08
ORD IDord-254ff9af9d7a4367b3dac3842ad7daa3
出典メモuspto-grants-2013_08