Water → 2-(Diethylamino-acetylamino)-6-(chloroacetylamino)-benzo[1,2-d:5,4-d']bisthiazole
Reaktionsgleichung
[Cl:1][CH2:2][C:3](Cl)=[O:4].[CH2:6]([N:8]([N:11]([C:25](=[O:27])[CH3:26])[C:12]1[S:13][C:14]2[C:15](=[CH:17][C:18]3[N:19]=[C:20]([NH2:24])[S:21][C:22]=3[CH:23]=2)[N:16]=1)[CH2:9][CH3:10])[CH3:7].O.N1C=CC=CC=1>CN(C)C=O>[CH2:6]([N:8]([N:11]([C:25](=[O:27])[CH3:26])[C:12]1[S:13][C:14]2[C:15](=[CH:17][C:18]3[N:19]=[C:20]([NH:24][C:3](=[O:4])[CH2:2][Cl:1])[S:21][C:22]=3[CH:23]=2)[N:16]=1)[CH2:9][CH3:10])[CH3:7]Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
500 mgm of chloroacetyl chloride were added to a stirred solution of 950 gm of 2-(diethylamino-acetylamino)6-amino-benzo[1,2-d:5,4-d']bisthiazole in 5 ml of dimethylformamide at 0° to 5° C. The mixture was heated for 30 minutes on a waterbath, then cooled, admixed with 50 ml of water and made alkaline with pyridine. The resulting precipitate was collected, washed and recrystallized from dimethylformamide.
Aufarbeitung
- temperatureThe mixture was heated for 30 minutes on a waterbath
- temperaturecooled
- customThe resulting precipitate was collected
- washwashed
- customrecrystallized from dimethylformamide
Quellen und Nachweise
- ORD-Eintrag
- ord-c4baac9bbe744accbb68142065b01f91
- Quelldatensatz
- uspto-grants-1982_08
- Patentnummer
- US04344946
Notizen zur Reaktion
Wird geladen…