Ethyl Acetate → HCID 178473725, Verbindung
Reaktionsgleichung
Cl.Cl.Cl.[NH:4]1[CH:8]=[C:7]([CH2:9][N:10]2[C:16]3[CH:17]=[CH:18][C:19]([C:21]4[CH:22]=N[CH:24]=[CH:25][CH:26]=4)=[CH:20][C:15]=3[CH2:14][N:13]([C:27](=[O:32])[C:28](F)(F)F)[CH:12]([CH2:33][C:34]3[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=3)[CH2:11]2)[N:6]=[CH:5]1.[Sn](Cl)[Cl:41].[C:43](OCC)(=O)C>>[ClH:41].[C:27]([N:13]1[CH2:14][C:15]2[CH:20]=[C:19]([C:21]3[CH:22]=[CH:43][CH:24]=[CH:25][CH:26]=3)[CH:18]=[CH:17][C:16]=2[N:10]([CH2:9][C:7]2[N:6]=[CH:5][NH:4][CH:8]=2)[CH2:11][C@H:12]1[CH2:33][C:34]1[CH:35]=[CH:36][CH:37]=[CH:38][CH:39]=1)(=[O:32])[CH3:28]Komponenten
4
Versuchsvorschrift
A mixture of Compound B (660 mg, 1.68 mmol), tin (II) chloride (1.52 g, 6.7 mmol) and ethyl acetate (75 mL) was stirred at room temperature for 18 hours and quenched with aqueous and then solid potassium carbonate (5 mL, then 5 gms). The mixture was filtered, the filtrate partitioned and the organic phase dried (MgSO4), concentrated in vacuum, and purified using flash chromatography (3:1 hexane:ethyl acetate) to provide Compound C (315 mg, 52%) as a clear oil.
Aufarbeitung
- customquenched with aqueous and then solid potassium carbonate (5 mL
- filtrationThe mixture was filtered
- customthe filtrate partitioned
- dry with materialthe organic phase dried (MgSO4)
- concentrationconcentrated in vacuum
- custompurified
Quellen und Nachweise
- ORD-Eintrag
- ord-68c0a6e5f2b94757874d08b924a83cff
- Quelldatensatz
- uspto-grants-2000_01
- Patentnummer
- US06011029
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