Reaktionsgleichung
[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[CH:10]([C:16]([O:18]CC)=O)[C:11]([O:13]CC)=O.[N:21]1([C:27](=[NH:29])[NH2:28])[CH2:26][CH2:25][O:24][CH2:23][CH2:22]1>C1(C)C=CC=CC=1>[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[C:10]1[C:11]([OH:13])=[N:28][C:27]([N:21]2[CH2:26][CH2:25][O:24][CH2:23][CH2:22]2)=[N:29][C:16]=1[OH:18]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture 1,3-diethyl 2-(1,3-benzothiazol-2-yl)propanedioate (3.00 g, 10.23 mmol, 1.00 equiv), and morpholine-4-carboximidamide (1.33 g, 10.30 mmol, 1.00 equiv) in Toluene (30 mL) was heated for 20 h at 120° C. under an inert atmosphere of nitrogen. After cooling down, the white solid was collected by filtration, washed with a mixture solution of Dichloromethane/Methanol and dried in an IR oven to afford the title compound. as a white solid. MS m/z [M+H]+ (ESI): 331.
Aufarbeitung
- temperatureAfter cooling down
- filtrationthe white solid was collected by filtration
- washwashed with a mixture solution of Dichloromethane/Methanol
- customdried in an IR oven
Quellen und Nachweise
- ORD-Eintrag
- ord-fc039b7d9efd457287a7034d818c6d6a
- Quelldatensatz
- uspto-grants-2015_12
- Patentnummer
- US09221809B2
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