戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 507366作成日:2026年10月25日

Malonic Acid → 2-(3-Hydroxy-5-iodo-2-oxo-2,3-dihydro-1H-indol-3-yl)-N,N-dimethyl-acetamide

https://huagongshe.com/reaction/507366

反応式

関与物質

役割名称HCID仕込み量
反応物Malonic AcidHCID 867—
反応物PyridineHCID 1049—
反応物Dimethylcarbamoyl ChlorideHCID 6598—
反応物IsatinHCID 7054—
反応物TriethylamineHCID 8471—
反応物5-IodoisatinHCID 88695—
反応物pyridinium (3-hydroxy-5-iodo-2-oxo-2,3-dihydro-1H-indol-3-yl)-acetateHCID 67148240—
溶媒Ethyl AcetateHCID 8857—
生成物2-(3-Hydroxy-5-iodo-2-oxo-2,3-dihydro-1H-indol-3-yl)-N,N-dimethyl-acetamideHCID 59129753—

反応条件

温度80 °C

反応手順

A 2 L flask with mechanical stirrer is charged with 5-iodo-isatin (78.1 g, 0.286 mol), malonic acid (35.7 g, 0.343 mol), and pyridine (90.4 g, 1.144 mol). The mixture is heated to 80° C. When most of the isatine has dissolved, ethyl acetate (100 mL) is added to prevent blocking of the stirrer by the precipitating pyridinium (3-hydroxy-5-iodo-2-oxo-2,3-dihydro-1H-indol-3-yl)-acetate. After 1 hour, precipitation of the latter salt starts, and when the mixture has been kept stirring for another 2 hours, a suspension of the salt in an orange solution has formed. To this is added triethyl amine (43.3 g, 0.429 mol), and the salt dissolves to give a dark solution. Then a solution of dimethyl carbamoyl chloride (40 g, 0.372 mol) in ethyl acetate (50 mL) is added dropwise during 20 minutes. A solid starts to precipitate, and the mixture is stirred for another 2 hours at 80° C. Then 4 N HCl is added (350 mL), and stirring is continued for 30 additional minutes in order to hydrolyze any excess carbamoyl chloride. The mixture is then filtered, and the filter cake is washed with 50% ethanol and then with water. After drying 72.6 g (70.5%) of a grayish powder of the title compound, mp.=246° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07786156B2
出典データセットuspto-grants-2010_08
ORD IDord-b0988c81260a4842bb0ba4f7623ce4ba
出典メモuspto-grants-2010_08