2(5H)-Thiazolone, 4-amino- → HCID 178509023, Verbindung
Reaktionsgleichung
[O:1]=[C:2]1[NH:6][C:5](=[NH:7])[CH2:4][S:3]1.[NH:8]=[C:9]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[C:11](=N)[NH:10]1>O>[NH:8]=[C:9]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[C:11](=[C:4]2[S:3][C:2](=[O:1])[NH:6][C:5]2=[NH:7])[NH:10]1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
11.4 parts of 2-oxo-4-iminothiazolidine are stirred with 15 parts of 1,3-diiminoisoindoline in 300 parts of water for 40 hours at about 25° C., whilst passing a slight stream of nitrogen over the mixture. The product is then filtered off and washed with water, giving 22 parts of 1-imino-3-(2'-oxo-4'-iminothiazolidinylidene)-isoindoline (Formula II, Z=>O), the spectroscopic properties of which correspond to those of the product obtained as described in Example 11.
Aufarbeitung
- filtrationThe product is then filtered off
- washwashed with water
Quellen und Nachweise
- ORD-Eintrag
- ord-7a15fb0b95d84aa5b5a89d949c6217ea
- Quelldatensatz
- uspto-grants-1982_03
- Patentnummer
- US04321390
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