5-(4-Chlorophenyl)methylene-3-[4-(imidazo[1,2-a]pyridin-5-ylthio)butyl]oxazolidine-2,4-dione → 5-(4-Chlorophenyl)methylene-3-[4-(imidazo[1,2-a]pyridin-5-ylthio)butyl]oxazolidine-2,4-dione hydrochloride

HRID 357177Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 357177
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]=[C:9]2[O:13][C:12](=[O:14])[N:11]([CH2:15][CH2:16][CH2:17][CH2:18][S:19][C:20]3[N:25]4[CH:26]=[CH:27][N:28]=[C:24]4[CH:23]=[CH:22][CH:21]=3)[C:10]2=[O:29])=[CH:4][CH:3]=1>CO.Cl>[ClH:1].[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]=[C:9]2[O:13][C:12](=[O:14])[N:11]([CH2:15][CH2:16][CH2:17][CH2:18][S:19][C:20]3[N:25]4[CH:26]=[CH:27][N:28]=[C:24]4[CH:23]=[CH:22][CH:21]=3)[C:10]2=[O:29])=[CH:6][CH:7]=1

Komponenten

4

Versuchsvorschrift

To a solution of 0.301 g (0.70 mmol) of 5-(4-chlorophenyl)methylene-3-[4-(imidazo[1,2-a]pyridin-5-ylthio)butyl]oxazolidine-2,4-dione in 10 ml of methanol, 0.10 ml of concentrated hydrochloric acid was added. After the solvent was distilled off, the residue was crystallized by the addition of diethyl ether to yield 0.223 g (68.6%, light pink crystal) of the desired product.

Aufarbeitung

  1. distillationAfter the solvent was distilled off
  2. customthe residue was crystallized by the addition of diethyl ether

Quellen und Nachweise

ORD-Eintrag
ord-ddfa37448dd64177b4b7a815fc9c0367
Quelldatensatz
uspto-grants-1998_11
Patentnummer
US05840732

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