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HRID 486669作成日:2026年10月26日

Chlorosuccinimide → 2-amino-5-chloro-N-methyl-alpha-(3-methyl-2-thienyl)benzeneethanamine

https://huagongshe.com/reaction/486669

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorosuccinimideHCID 31398—
反応物Compound 7189HCID 130176—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
生成物2-amino-5-chloro-N-methyl-alpha-(3-methyl-2-thienyl)benzeneethanamineHCID 1006223311.5%

反応手順

A stirred solution of 8 g of 2-amino-N-methyl-α-(3-methyl-2-thienyl)benzeneethanamine in 40 ml of N,N-dimethylformamide was treated with a solution of 6.41 g of N-chlorosuccinimide in 40 ml of N,N-dimethylformamide and then stirred at room temperature for 8 hours. Evaporation of the volatiles afforded an oil which was decanted into 100 ml of water, basified with 30 ml of 10% aqueous sodium hydroxide and extracted with dichloromethane (2×100 ml). The extract was washed with water (2×100 ml), dried over anhydrous sodium sulfate and concentrated. Thin layer chromatography of the resultant oil indicated a multicomponent mixture. Purification of the mixture was accomplished by successive HPLC separations (Water's Associates Prep LC/System 500, silica gel, elution with methanol). Concentration of the appropriate fractions afforded a residue which was dissolved in diethyl ether, filtered free of insolubles and concentrated. The resultant oil crystallized upon standing to yield 1.05 g of 2-amino-5-chloro-N-methyl-α-(3-methyl-2-thienyl)benzeneethanamine, mp 59°-61° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05292760
出典データセットuspto-grants-1994_03
ORD IDord-dff2f7e39068414cb4ed04eb86478962
出典メモuspto-grants-1994_03