Bromo-4'-chloro-3'-sulfamoylacetophenone → 4-(4-Chloro-3-sulfamoylphenyl)-2-isobutylimino-3-methyl-1,3-thiazolidine-4-ol-hydrobromide

HRID 461122

Reaktionsgleichung

Reaktionsgleichung von HRID 461122
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:11])[CH2:9][Br:10])=[CH:4][C:3]=1[S:12](=[O:15])(=[O:14])[NH2:13].[CH2:16]([NH:20][C:21]([NH:23][CH3:24])=[S:22])[CH:17]([CH3:19])[CH3:18]>>[BrH:10].[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2([OH:11])[CH2:9][S:22][C:21](=[N:20][CH2:16][CH:17]([CH3:19])[CH3:18])[N:23]2[CH3:24])=[CH:4][C:3]=1[S:12](=[O:15])(=[O:14])[NH2:13]

Komponenten

3

Edukt 2

HCID 12952390Bromo-4'-chloro-3'-sulfamoylacetophenoneHCID 155682431-Isobutyl-3-methylthiourea

Produkt 1

HCID 227604724-(4-Chloro-3-sulfamoylphenyl)-2-isobutylimino-3-methyl-1,3-thiazolidine-4-ol-hydrobromide

Versuchsvorschrift

6.2 g of 4'-chloro-3'-sulfamoyl-2-bromoacetophenone and 3.0 g of 1-isobutyl-3-methylthiourea were reacted according to the prescription made in Example 23 and the colorless end product was precipitated with 200 ml of diethyl ether.

Aufarbeitung

  1. customthe colorless end product was precipitated with 200 ml of diethyl ether

Quellen und Nachweise

ORD-Eintrag
ord-3030b07c7e8244d4aca4cef3dee0274f
Quelldatensatz
uspto-grants-1977_12
Patentnummer
US04061761

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