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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1420044Erstellt: 25. Oktober 2026

Water → N-[4-(5H-pyrrolo[2,1-c][1,4]benzodiazepin-10(11H)ylcarbonyl)-3-chlorophenyl]-3-fluoro-2-methylbenzamide

https://huagongshe.com/reaction/1420044

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktDiisopropylethylamineHCID 81531—
EduktBenzoyl chloride, 2-chloro-4-[(5-fluoro-2-methylbenzoyl)amino]-HCID 10639786—
Edukt10,11-Dihydro-5H-benzo[e]pyrrolo[1,2-a][1,4]diazepineHCID 15547048—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-[4-(5H-pyrrolo[2,1-c][1,4]benzodiazepin-10(11H)ylcarbonyl)-3-chlorophenyl]-3-fluoro-2-methylbenzamideHCID 10672170—

Reaktionsschritte

To a solution of 1.50 g of 10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine in 25 ml of methylene chloride is added 1.23 g of N,N-diisopropylethylamine. While cooling in an ice bath, a solution of 3.08 g of [4-[(2-methyl-5-fluorobenzoyl)amino]-2-chlorobenzoyl chloride in 50 ml of methylene chloride is added. The reaction mixture becomes homogeneous and is stirred at room temperature for 18 hours. Water is added and the separated organic layer washed with saturated sodium bicarbonate, dried with Na2SO4 and passed through a short pad of hydrous magnesium silicate two times. The methylene chloride is removed in vacuo to give 3.81 g of a glass. A sample is crystallized from ethyl acetate to give crystalline solid, m.p. 200°-205° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05889001
Quelldatensatzuspto-grants-1999_03
ORD IDord-bf449e37b00d493eb09f043d5af45240
Quellennotizuspto-grants-1999_03