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HRID 1729968作成日:2026年10月27日

2-Methylamino-5-nitrobenzophenone → Nimetazepam

https://huagongshe.com/reaction/1729968

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methylamino-5-nitrobenzophenoneHCID 78661—
反応物2-Isocyanatoacetyl chlorideHCID 13229176—
溶媒WaterHCID 962—
生成物NimetazepamHCID 4496—

反応条件

温度95 °C

反応手順

2-Milliliters of 2-isocyanatoacetyl chloride was cooled, and 0.20 g. of powdered 2-methylamino-5-nitrobenzophenone was added thereto with stirring. After stirring the resulting mixture at room temperature for one hour, excess 2-isocyanatoacetyl chloride was removed by reduced pressure distillation. To the residue was added 4 ml. of pyridine, whereby a reaction took place with generation of heat. The reaction liquid was heated at 95° C, for 1.5 hours, diluted with water and then extracted with chloroform. The chloroform layer was washed with a 5% aqueous hydrochloric acid solution and then with an aqueous sodium chloride solution in this order, dried over Glauber's salt, and evaporated by reduced pressure distillation. Subsequently, the residue was chromatographically purified (solvent: chloroform→ethyl acetate) by use of a column packed with 10 g. of silica gel to obtain 1-methyl-5-phenyl-7-nitro-1,3-dihydro-2H-1,4-benzodiazepin-2-one having a melting point of 154° to 156° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03991048
出典データセットuspto-grants-1976_11
ORD IDord-442193375f16488eb44e92ef81577abc
出典メモuspto-grants-1976_11