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HRID 2379480作成日:2026年10月25日

Triethylamine → 4-(2-Chlorophenyl)-3-(3,5-di-tert-butyl-4-hydroxybenzamido)-6,8-dimethylquinoline

https://huagongshe.com/reaction/2379480

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物3,5-Di-tert-butyl-4-hydroxybenzoic acidHCID 15007—
反応物3-Amino-4-(2-chlorophenyl)-6,8-dimethylquinolineHCID 10446536—
反応物DiethylphosphorylcyanideHCID 13586794—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物4-(2-Chlorophenyl)-3-(3,5-di-tert-butyl-4-hydroxybenzamido)-6,8-dimethylquinolineHCID 1523062424.2%

反応条件

温度0 °C

反応手順

To a mixture of 3-amino-4-(2-chlorophenyl)-6,8-dimethylquinoline (1.02 g), 3,5-di-tert-butyl-4-hydroxy benzoic acid (750 mg), diethylphosphoryl cyanide (DEPC) (587 mg) and N,N-dimethylformamide (100 mg) was dropwise added a solution of triethylamine (0.51 ml) in DMF (2 ml) under stirring at 0° C. The mixture was stirred at 0° C. for 30 minutes and at room temperature for one night. Then, the mixture was diluted with water and extracted with ethyl acetate. The ethyl acetate layer was concentrated after being washed with water and dried (MgSO4). The residue was purified by a silica gel column chromatography with hexane-ethyl acetate (85:15,V/V), and then crystallized from methanol to give 4-(2-chlorophenyl)-3-(3,5-di-tert-butyl-4-hydroxybenzamido)-6,8-dimethylquinoline (373 mg, 24.2%). Recrystallization from methanol gave colorless prisms of mp 127°-129° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05362742
出典データセットuspto-grants-1994_11
ORD IDord-75204cccb2f74fafa026fa5af2ebb21d
出典メモuspto-grants-1994_11