Ammonia → 5-dimethylamino-N-(5-cyano-6-ethyl-2,1,3-benzoxadiazol-4-yl)-1-naphthalenesulfonamide

HRID 1622

Reaktionsgleichung

Reaktionsgleichung von HRID 1622
[CH3:1][N:2]([CH3:29])[C:3]1[CH:12]=[CH:11][CH:10]=[C:9]2[C:4]=1[CH:5]=[CH:6][CH:7]=[C:8]2[S:13]([NH:16][C:17]1[C:25]2[C:21](=[N:22][O:23][N:24]=2)[CH:20]=[C:19]([CH2:26][CH3:27])[C:18]=1Br)(=[O:15])=[O:14].[Cu](C#N)[C:31]#[N:32].N>N1C=CC=CC=1>[CH3:1][N:2]([CH3:29])[C:3]1[CH:12]=[CH:11][CH:10]=[C:9]2[C:4]=1[CH:5]=[CH:6][CH:7]=[C:8]2[S:13]([NH:16][C:17]1[C:25]2[C:21](=[N:22][O:23][N:24]=2)[CH:20]=[C:19]([CH2:26][CH3:27])[C:18]=1[C:31]#[N:32])(=[O:15])=[O:14]

Komponenten

5

Versuchsvorschrift

A mixture of 4.6 g of 5-dimethylamino-N-(5-bromo-6-ethyl-2,1,3-benzoxadiazol-4-yl)-1-naphthalenesulfonamide and 1.3 g of copper cyanide is heated for 8 hours at 120° in 30 ml of pyridine. The mixture is poured onto aqueous ammonia solution, worked up in the customary manner and 5-dimethylamino- N-(5-cyano-6-ethyl-2,1,3-benzoxadiazol-4-yl)-1-naphthalenesulfonamide is obtained.

Quellen und Nachweise

ORD-Eintrag
ord-7917d2b512334ae09464c8fd110ae2ba
Quelldatensatz
uspto-grants-1998_03
Patentnummer
US05726194

Verknüpfte Notizen

Wird geladen…