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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2218627Erstellt: 26. Oktober 2026

5-bromomethylene-10,11-dihydro-5H-dibenzo[a,d]cycloheptene → N-[3-(10,11-Dihydro-dibenzo[a,d]cyclohepten-5-ylidenemethyl)-2-methyl-phenyl]-methanesulfonamide

https://huagongshe.com/reaction/2218627

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-bromomethylene-10,11-dihydro-5H-dibenzo[a,d]cyclohepteneHCID 5257940—
EduktN-[2-methyl-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-methanesulfonamideHCID 58613440—
ProduktN-[3-(10,11-Dihydro-dibenzo[a,d]cyclohepten-5-ylidenemethyl)-2-methyl-phenyl]-methanesulfonamideHCID 5976989513,2%

Reaktionsschritte

Following the procedures essentially as described in Example 219, below, and using N-[2-methyl-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-methanesulfonamide (120 mg, 0.386 mmol) and 5-bromomethylene-10,11-dihydro-5H-dibenzo[a,d]cycloheptene (100 mg, 0.351 mmol), purification by UV-guided semi-preparatory reverse-phase HPLC affords 18 mg (13%) of the title compound as a yellow oil. MS (ES) 407 M+NH4), 388 (M−H); HPLC shows 96% purity.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07411072B2
Quelldatensatzuspto-grants-2008_08
ORD IDord-0ef03af8d4414d6a8244f0a33dbcaed7
Quellennotizuspto-grants-2008_08