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HRID 1735242作成日:2026年10月27日

Triethylamine → N-[5-(5H-Pyrrolo[2,1-c][1,4]benzodiazepin-10(11H)ylcarbonyl)-2-pyridinyl]-2-methylbenzeneacetamide

https://huagongshe.com/reaction/1735242

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物o-Tolyl-acetyl chlorideHCID 2760632—
反応物10, 11-dihydro-10-(6-amino-3-pyridinylcarbonyl)-5H-pyrrolo[2,1-c][1,4]benzodiazepineHCID 18917501—
溶媒DichloromethaneHCID 6344—
生成物N-[5-(5H-Pyrrolo[2,1-c][1,4]benzodiazepin-10(11H)ylcarbonyl)-2-pyridinyl]-2-methylbenzeneacetamideHCID 18917528—

反応手順

A mixture of 2.0 mmol of 10, 11-dihydro-10-(6-amino-3-pyridinylcarbonyl)-5H-pyrrolo[2,1-c][1,4]benzodiazepine, 2.1 mmol of 2-methylbenzeneacetyl chloride and 5 mmol of triethylamine in 10 ml of dichloromethane is stirred under argon at room temperature for 16 hours. The solvent is removed under vacuum and the residue partitioned between 50 ml of ethyl acetate and 25 ml of water. The organic layer is separated, washed with H2O, 1N NaHCO3, brine and dried (Na2SO4). The solvent is removed and the residue chromatographed on silica gel with ethyl acetate-hexane as solvent to give the product as a solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05536718
出典データセットuspto-grants-1996_07
ORD IDord-fa9ad543ba63442b81d2d3bbf3850ef4
出典メモuspto-grants-1996_07