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HRID 1925457作成日:2026年10月24日

Triethylamine → N1-(2-chloro-3-nitroquinolin-4-yl)-2-methylpropane-1,2-diamine

https://huagongshe.com/ja/reaction/1925457

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2-MethylpropylenediamineHCID 13128—
反応物2,4-Dichloro-3-nitroquinolineHCID 2785138—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物N1-(2-chloro-3-nitroquinolin-4-yl)-2-methylpropane-1,2-diamineHCID 8622776599.9%

反応条件

温度0 °C

反応手順

Under a nitrogen atmosphere, triethylamine (6.6 mL, 47 mmol) was added slowly to a solution of 2,4-dichloro-3-nitroquinoline (10.0 g, 41.1 mmol) in anhydrous 1-methyl-2-pyrrolidinone (40 mL). The reaction mixture was cooled to 0° C. with an ice bath. A solution of 1,2-diamino-2-methylpropane (4.1 g, 47.3 mmol) in anhydrous 1-methyl-2-pyrrolidinone (5 mL) was added dropwise over a period of 15 minutes while maintaining the temperature of the reaction mixture below 4° C. After the addition was completed the ice bath was removed and the reaction mixture was allowed to stir at ambient temperature for 4 hours. The reaction mixture was slowly poured into vigorously stirred warm water (300 mL). The resulting suspension was stirred for 1 hour and then cooled to 13° C. by adding ice. The solid was isolated by filtration and then washed with cold water until the filtrate was clear to provide 12.1 g of N1-(2-chloro-3-nitroquinolin-4-yl)-2-methylpropane-1,2-diamine as a damp yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08178677B2
出典データセットuspto-grants-2012_05
ORD IDord-bde88d1493ca41b491bcb3f6d7f47df5
出典メモuspto-grants-2012_05