Reaktionsgleichung
[F:1][C:2]1[CH:3]=[C:4]([CH:6]=[CH:7][C:8]=1[N:9]1[CH2:14][CH2:13][O:12][CH2:11][CH2:10]1)[NH2:5].[CH2:15]1[O:17][C@H:16]1[CH2:18][Cl:19]>C(O)(C)C>[Cl:19][CH2:18][C@H:16]([OH:17])[CH2:15][NH:5][C:4]1[CH:6]=[CH:7][C:8]([N:9]2[CH2:14][CH2:13][O:12][CH2:11][CH2:10]2)=[C:2]([F:1])[CH:3]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
3-Fluoro-4-morpholinyl aniline (39 g) is mixed with R-epichlorohydrin (18.5 g), isopropyl alcohol (200 ml) is added and heated for 16 hours at reflux temperature. The solvent is distilled to give 57 gm of N-[3-Chloro-2-(R)-hydroxypropyl]-3-fluoro-4-morpholinyl aniline.
Aufarbeitung
- additionis added
- temperatureheated for 16 hours
- temperatureat reflux temperature
- distillationThe solvent is distilled
Quellen und Nachweise
- ORD-Eintrag
- ord-be059e33dcdc4ec49c1e9eb1e2a24b02
- Quelldatensatz
- uspto-grants-2010_06
- Patentnummer
- US07741480B2
Verknüpfte Notizen
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