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HRID 3593作成日:2026年10月23日

Dimethylamine → alpha-(Dimethylamino)-N-[4-(5H-pyrrolo[2,1-c][1,4]benzodiazepin-10(11H)-ylcarbonyl)phenyl]benzeneacetamide

https://huagongshe.com/ja/reaction/3593

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylamineHCID 674—
反応物2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
反応物Ethyl acetate hexaneHCID 21226206—
反応物alpha-Chloro-N-[4-(5H-pyrrolo[2,1-c][1,4)benzodiazepin-10(11H)-ylcarbonyl)phenyl]benzeneacetamideHCID 21837022—
溶媒MethanolHCID 887—
生成物alpha-(Dimethylamino)-N-[4-(5H-pyrrolo[2,1-c][1,4]benzodiazepin-10(11H)-ylcarbonyl)phenyl]benzeneacetamideHCID 21837078—

反応手順

A partial solution of ?? g of α-chloro-N-[4-(5H-pyrrolo[2,1-c][1,4]benzodiazepin-10(11H)-ylcarbonyl)phenyl]benzeneacetamide in 1 ml of methanol is treated with 0.5 ml of dimethylamine and 1 ml of 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone and stirring continued for 20 hours. The methanol is evaporated and the residue diluted with water. The resulting solid is washed with water, dissolved in ethyl acetate and the organic layer washed with saturated NaHCO3, brine and dried with Na2SO4. The mixture is filtered and the filtrate evaporated in vacuo to give a residue which is stirred with ethyl acetate-hexane to give 0.15 g of a beige solid. MS(CI): 465 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05733905
出典データセットuspto-grants-1998_03
ORD IDord-10007385ab964c208a8b83d8c610f4fa
出典メモuspto-grants-1998_03