Benzo(d)thiazol-2-amine → HCID 60143342, Verbindung
Reaktionsgleichung
[NH2:1][C:2]1[S:3][C:4]2[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=2[N:6]=1.C(N=C=NCCCN(C)C)C.ON1C2C=CC=CC=2N=N1.[CH3:32][O:33][C:34]1[CH:44]=[CH:43][C:42](/[CH:45]=[CH:46]\[C:47]2[CH:52]=[C:51]([O:53][CH3:54])[C:50]([O:55][CH3:56])=[C:49]([O:57][CH3:58])[CH:48]=2)=[CH:41][C:35]=1[O:36][CH2:37][C:38](O)=[O:39]>ClCCl.O>[S:3]1[C:4]2[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=2[N:6]=[C:2]1[NH:1][C:38](=[O:39])[CH2:37][O:36][C:35]1[CH:41]=[C:42](/[CH:45]=[CH:46]\[C:47]2[CH:52]=[C:51]([O:53][CH3:54])[C:50]([O:55][CH3:56])=[C:49]([O:57][CH3:58])[CH:48]=2)[CH:43]=[CH:44][C:34]=1[O:33][CH3:32]Komponenten
7
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
To a solution of 2-aminobenzothiazole (150 mg, 1.0 mmol) in dichloromethane (20 mL) was added 1-Ethyl-3-(3-Dimethylaminopropyl)carbodiimide (EDC) (191 mg, 1.0 mmol) and 1-hydroxy-1,2,3-benzotriazole (HOBt) (13.5 mg, 0.1 mmol). Then added 2-{2-methoxy-5-[(Z)-2-(3,4,5-trimethoxyphenyl)-1-ethenyl]phenoxy}acetic acid (1) (374 mg, 1.0 mmol) and the reaction mixture was stirred at a temperature of 25° C. for 24 h and the reaction was monitored by TLC. Then to this water is added and extracted with dichloromethane. The solvent was evaporated under vacuum to afford the crude product. This was further purified by column chromatography using ethyl acetate and hexane as solvent system to obtain the pure product (8a) (395 mg, 80% yield).
Aufarbeitung
- extractionextracted with dichloromethane
- customThe solvent was evaporated under vacuum
- customto afford the crude product
- customThis was further purified by column chromatography
Quellen und Nachweise
- ORD-Eintrag
- ord-89e5bfc981e54552ad5517d8eff01d44
- Quelldatensatz
- uspto-grants-2015_08
- Patentnummer
- US09102638B2
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