Reaktionsgleichung
Cl[C:2]1([CH2:7][C:8]([Cl:11])([Cl:10])Cl)[O:5][C:4](=[O:6])[CH2:3]1.[NH:12]1[CH2:17][CH2:16][O:15][CH2:14][CH2:13]1.C([O-])(O)=O.[Na+]>C(Cl)Cl.CC(OC)(C)C>[Cl:11][C:8]([Cl:10])=[CH:7][C:2](=[O:5])[CH2:3][C:4]([N:12]1[CH2:17][CH2:16][O:15][CH2:14][CH2:13]1)=[O:6]Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Reaktionsbedingungen
- Temperatur
- 15 °C
Versuchsvorschrift
Two separate solutions of 1 (62.5 g, 0.26 mmol) and morpholine (24.0 g, 0.28 mol) in DCM (120 ml) were added simultaneously to a mixture of NaHCO3 (44.0 g, 0.52 mol) in dry DCM (300 ml). The reaction was maintained at 15° C. over 140 minutes with stirring. The reaction was filtered, washed with DCM (3×100 ml) and the combined organic layers were concentrated in vacuo to a slurry which was then passed through a short silica pad, and further washed with DCM (4×100 ml). The combined organic layers were concentrated in vacuo, suspended in hexane (400 ml) and stirred for 1 hour, filtered and dried to give a cream solid. The solid was suspended in TBME (100 ml), stirred for 15 minutes, filtered, washed with TBME and dried to give 2 as a white powder (47.8 g, 72%). m/z (LC-MS, ESP): 252 (M++1).
Aufarbeitung
- filtrationThe reaction was filtered
- washwashed with DCM (3×100 ml)
- concentrationthe combined organic layers were concentrated in vacuo to a slurry which
- washfurther washed with DCM (4×100 ml)
- concentrationThe combined organic layers were concentrated in vacuo
- stirringstirred for 1 hour
- filtrationfiltered
- customdried
- customto give a cream solid
- stirringstirred for 15 minutes
- filtrationfiltered
- washwashed with TBME
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-d7bb44506c7b4f79a57d2e5895c64e63
- Quelldatensatz
- uspto-grants-2006_05
- Patentnummer
- US07049313B2
Verknüpfte Notizen
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