Sodium Iodide → 2'-Isobutyl-4-methylvalerohydrazide
Reaktionsgleichung
ClCCCS([N:8]([CH2:37][CH:38]([CH3:40])[CH3:39])[NH:9][C:10](=[O:36])[C@@H:11]([C@@H](C(=O)NOC1CCCCO1)C/C=C/C1C=CC=CC=1)[CH2:12][CH:13]([CH3:15])[CH3:14])(=O)=O.[I-].[Na+].C(NCC)C>C(C(C)=O)C.C(OCC)(=O)C>[CH2:37]([NH:8][NH:9][C:10](=[O:36])[CH2:11][CH2:12][CH:13]([CH3:15])[CH3:14])[CH:38]([CH3:40])[CH3:39]Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Reaktionsbedingungen
- Temperatur
- 80 °C
Versuchsvorschrift
A solution of 0.60 g of (E)-2′-(3-chloropropylsulphonyl)-2(R)-[1(S)-[(tetrahydro-2(RS)-pyranyloxy)carbamoyl]-4-phenyl-3-butenyl]-2′-isobutyl-4-methylvalerohydrazide in 10 ml of methyl ethyl ketone was treated with 0.18 g of sodium iodide and 1.04 ml of diethylamine. The mixture was heated at 80° C. for 4 hours and then at 60° C. for 48 hours. The mixture was diluted with ethyl acetate, washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulphate and evaporated. The residue was purified by column chromatography on silica gel using methanol/dichloromethane (1:9) for the elution to give 0.16 g of (E)-2′-[3-(diethylamino)propylsulphonyl]-2(R) -[1(S)-(tetrahydro-2(RS)-pyranyloxy)carbamoyl]-4-phenyl-3-butenyl]-2′-isobutyl-4-methylvalerohydrazide in the form of a gum.
Aufarbeitung
- washwashed with water and saturated aqueous sodium chloride
- dry with materialdried over anhydrous magnesium sulphate
- customevaporated
- customThe residue was purified by column chromatography on silica gel
- washfor the elution
Quellen und Nachweise
- ORD-Eintrag
- ord-aa5eec3e35e3463bbf7efb9f8ee4d054
- Quelldatensatz
- uspto-grants-2001_07
- Patentnummer
- US06265446B1
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