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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 976406Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/976406

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukto-Tolyl-acetyl chlorideHCID 2760632—
Edukt10, 11-dihydro-10-(6-amino-3-pyridinylcarbonyl)-5H-pyrrolo[2,1-c][1,4]benzodiazepineHCID 18917501—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-[5-(5H-Pyrrolo[2,1-c][1,4]benzodiazepin-10(11H)ylcarbonyl)-2-pyridinyl]-2-methylbenzeneacetamideHCID 18917528—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05612334
Quelldatensatzuspto-grants-1997_03
ORD IDord-08f31ee8f77a4599b0ad743ed3bda9b7
Quellennotizuspto-grants-1997_03