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HRID 962597Erstellt: 25. Oktober 2026

Triethylamine → N-[4-[(5,11-dihydro-10H-dibenz[b,e](1,4]diazepin-5-yl)carbonyl]phenyl]-2-methylbenzamide

https://huagongshe.com/reaction/962597

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt10,11-Dihydro-5h-dibenzo[b,e][1,4]diazepineHCID 36046—
Edukt4-[(2-methylbenzoyl)amino]benzoyl ChlorideHCID 10707441—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-[4-[(5,11-dihydro-10H-dibenz[b,e](1,4]diazepin-5-yl)carbonyl]phenyl]-2-methylbenzamideHCID 67624893—

Reaktionsschritte

A mixture of 1.0 g of 5,11-dihydro-10H-dibenz [b,e] [1,4]diazepine 1.9 g of 4-[(2-methylbenzoyl) amino]benzoyl chloride, 4 ml of triethylamine and 0.2 g of 4-(dimethylamino)pyridine in 60 ml of methylene chloride is stirred at room temperature for 18 hours. The reaction mixture is poured into ice water and the separated organic layer washed with 50 ml each of water, 2N HCl, water, saturated NaHCO3 and water. The organic layer is dried (Na2SO4) and the solvent removed to give a residue. The residue is chromatographed on a silica gel column using 1:4 ethyl acetate-hexane to give 1.8 g of the desired product as a solid, m.p. 68°-71° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05760031
Quelldatensatzuspto-grants-1998_06
ORD IDord-18fe0cefdc9e437f9590799a74919879
Quellennotizuspto-grants-1998_06