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HRID 25064作成日:2026年10月27日

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

https://huagongshe.com/reaction/25064

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物ChloroacetoneHCID 6571—
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WaterHCID 962—
生成物(+/-)-8-Methyl-7-(4-methyl-thiazol-2-yl)-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepineHCID 1213742382.5%

反応条件

温度85 °C

反応手順

A mixture of 0.76 g (1.98 mmol) of the starting material I, 1.10 g (11.88 mmol) of chloroacetone and 15 ml of dimethylformamide was stirred at 80-90° C. for 40 min. Then the reaction mixture was diluted with water, the precipitated crystals were filtered off, dried and purified by refluxing in ethanol to yield 0.69 g (82%) of the title compound; Mp.: 188-189° 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-9acdb13ea24346d98b1bb6f6e7dc3742
出典メモuspto-grants-2005_02