Reaktionsgleichung
[S:1]([C:4]1[CH:22]=[CH:21][C:7]2[N:8]=[C:9]([NH:11][C:12](=[O:20])OC3C=CC=CC=3)[S:10][C:6]=2[CH:5]=1)[C:2]#[N:3].[CH3:23][C@H:24]1[O:29][C@@H:28]([CH3:30])[CH2:27][N:26]([CH2:31][CH2:32][NH2:33])[CH2:25]1>>[CH3:30][C@H:28]1[O:29][C@@H:24]([CH3:23])[CH2:25][N:26]([CH2:31][CH2:32][NH:33][C:12]([NH:11][C:9]2[S:10][C:6]3[CH:5]=[C:4]([S:1][C:2]#[N:3])[CH:22]=[CH:21][C:7]=3[N:8]=2)=[O:20])[CH2:27]1Komponenten
3
Versuchsvorschrift
The 2-[({2-[(2R,6S)-2,6-dimethylmorpholin-4-yl]ethyl}carbamoyl)amino]-1,3-benzothiazol-6-yl thiocyanate was prepared according to the method described in Example 9c, but using 654 mg of phenyl (6-thiocyanato-1,3-benzothiazol-2-yl)carbamate and 0.35 cm3 of 2-[(2R,6S)-2,6-dimethylmorpholin-4-yl]ethanamine. 783 mg of 2-[({2-[(2R,6S)-2,6-dimethylmorpholin-4-yl]ethyl}carbamoyl)amino]-1,3-benzothiazol-6-yl thiocyanate are thus obtained in the form of a white solid, the characteristics of which are as follows:
Aufarbeitung
- customThe 2-[({2-[(2R,6S)-2,6-dimethylmorpholin-4-yl]ethyl}carbamoyl)amino]-1,3-benzothiazol-6-yl thiocyanate was prepared
Quellen und Nachweise
- ORD-Eintrag
- ord-8b8e1862e245442fb1dea22a3251896e
- Quelldatensatz
- uspto-grants-2016_04
- Patentnummer
- US09321777B2
Verknüpfte Notizen
Wird geladen…