戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1786925作成日:2026年10月25日

N-methyl-2-pyrrolidone → N-[4-(benzyloxy)-3-chlorophenyl]-5H-pyrrolo[3,2-d]pyrimidin-4-amine

https://huagongshe.com/reaction/1786925

反応式

関与物質

役割名称HCID仕込み量
反応物N-methyl-2-pyrrolidoneHCID 13387—
反応物4-Benzyloxy-3-chloroanilineHCID 1268285—
反応物4-chloro-5H-pyrrolo[3,2-d]pyrimidineHCID 5370695—
溶媒MethanolHCID 887—
生成物N-[4-(benzyloxy)-3-chlorophenyl]-5H-pyrrolo[3,2-d]pyrimidin-4-amineHCID 5759727149.5%

反応条件

温度80 °C

反応手順

A mixture of 4-chloro-5H-pyrrolo[3,2-d]pyrimidine (200 mg), 4-(benzyloxy)-3-chloroaniline (365 mg) and 1-methyl-2-pyrrolidone (3 mL) was stirred at 80° C. for 4 hrs. Methanol and activated carbon were added to the reaction mixture and the mixture was stirred. The activated carbon was filtered off, aqueous sodium hydrogen carbonate solution was added and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (eluent, methanol:ethyl acetate=0:100→15:75) and recrystallized from ethanol-ethyl acetate to give the title compound (226 mg) as a pale-brown powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07507740B2
出典データセットuspto-grants-2009_03
ORD IDord-69cd76e25f794ae5ae52dfdfac3d9ec8
出典メモuspto-grants-2009_03