Chloroform → HCID 46235731, Verbindung

HRID 1925184Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1925184
C(Cl)(Cl)Cl.[SH:5][C:6]1[C:7]([NH:16][C:17]([C:19]2([CH2:25][CH:26]([CH2:29][CH3:30])[CH2:27][CH3:28])[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]2)=[O:18])=[CH:8][C:9]2[C:14]([CH:15]=1)=[CH:13][CH:12]=[CH:11][CH:10]=2.[C:31](Cl)(=[O:35])[CH:32]([CH3:34])[CH3:33]>N1C=CC=CC=1>[CH2:27]([CH:26]([CH2:29][CH3:30])[CH2:25][C:19]1([C:17]([NH:16][C:7]2[C:6]([S:5][C:31](=[O:35])[CH:32]([CH3:34])[CH3:33])=[CH:15][C:14]3[C:9]([CH:8]=2)=[CH:10][CH:11]=[CH:12][CH:13]=3)=[O:18])[CH2:20][CH2:21][CH2:22][CH2:23][CH2:24]1)[CH3:28]

Komponenten

5

Versuchsvorschrift

To a chloroform solution of the product obtained in step B) are added 1.05 mol equivalents of isobutyryl chloride and 2.5 mol equivalents of pyridine at room temperature. The mixture is stirred for 1 hour, concentrated and then n-hexane is added. The solids are filtered off and the filtrate is concentrated. The remaining residue is purified by silica gel column chromatography to obtain the desired title compound.

Aufarbeitung

  1. concentrationconcentrated
  2. additionn-hexane is added
  3. filtrationThe solids are filtered off
  4. concentrationthe filtrate is concentrated
  5. customThe remaining residue is purified by silica gel column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-3a4df17bdfa34ba6843680b713f5177e
Quelldatensatz
uspto-grants-2012_05
Patentnummer
US08178583B2

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