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HRID 25070作成日:2026年10月27日

Dimethylformamide → (+/-)-7-(5,6-Dihydro-4-oxo-4H-1,3-thiazin-2-yl)-8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine

https://huagongshe.com/reaction/25070

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Ethyl 3-bromopropionateHCID 68320—
反応物(+/-)-8-Methyl-5-(4-nitrophenyl)-7-thiocarbamoyl-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepineHCID 12137394—
溶媒Sodium ChlorideHCID 5234—
生成物(+/-)-7-(5,6-Dihydro-4-oxo-4H-1,3-thiazin-2-yl)-8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepineHCID 2256550259%

反応条件

温度85 °C

反応手順

A mixture of 2.00 g (5.20 mmol) of the starting material I, 1.89 g (10.44 mmol) of ethyl 3-bromopropionate and 20 ml of dimethylformamide was stirred at 80-90° C. for 3 h. The reaction mixture was diluted with 25% sodium chloride solution and extracted with dichloromethane. After drying and concentration the crude product was purified by column chromatography using silica gel (MN Kieselgel 60) as adsorbent and a mixture of ethyl acetate-methanol (2:1) as eluent to yield 1.34 g (59%) of the title compound; Mp.: 220-221° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06858605B2
出典データセットuspto-grants-2005_02
ORD IDord-6e91e6ae17d04701a181c4bd260236a7
出典メモuspto-grants-2005_02