戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 8788作成日:2026年10月24日

Acetyl chloride → N[5-(4-Chlorophenyl)-6-(2,4-dichlorophenyl)-2-(2,2-dimethylpropanoyl)furo[2,3-b]pyridin-3yl]acetamide

https://huagongshe.com/ja/reaction/8788

反応式

関与物質

役割名称HCID仕込み量
反応物Acetyl chlorideHCID 6367—
反応物TriethylamineHCID 8471—
反応物1-(3-Amino-5-(4-chlorophenyl)-6-(2,4-dichlorophenyl)furo[2,3-b]pyridin-2-yl)-2,2-dimethylpropan-1-oneHCID 10254284—
溶媒DichloromethaneHCID 6344—
生成物N[5-(4-Chlorophenyl)-6-(2,4-dichlorophenyl)-2-(2,2-dimethylpropanoyl)furo[2,3-b]pyridin-3yl]acetamideHCID 10481643—

反応手順

A solution of 0.050 g (0.106 mmol) of the product from Example 17 in CH2Cl2 (1 mL) at 0° C. was treated with acetyl chloride (8 μL; 0.106 mmol) followed by triethylamine (15 μL; 0.106 mmol). After the addition, the reaction mixture was warmed to RT and stirred for 1 hour. The reaction was quenched with saturated NaHCO3 solution. The reaction mixture was partitioned between ethyl acetate and saturated NaHCO3 solution. The organic layer was washed twice with saturated NaHCO3 solution, brine, dried (Na2SO4), filtered, and concentrated in vacuo. Purification by MPLC (silica gel; 0% to 20% ethyl acetate-hexane gradient) gave the title compound. HPLC/MS: 515.0 (M+1), 517.0 (M+3); Rt=4.94 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091216B2
出典データセットuspto-grants-2006_08
ORD IDord-abf83597ba6e4559a8be72219905d54c
出典メモuspto-grants-2006_08