Hydrochloric Acid → 4-(6-Acetylaminomethylpyridin-2-yl)-2-(diaminomethyleneamino)thiazole dihydrochloride

HRID 2379848Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2379848
[ClH:1].[C:2]([NH:5][CH2:6][C:7]1[N:12]=[C:11]([C:13]2[N:14]=[C:15]([N:18]=[C:19]([NH2:21])[NH2:20])[S:16][CH:17]=2)[CH:10]=[CH:9][CH:8]=1)(=[O:4])[CH3:3].C(OC(C)C)(C)C>CO>[ClH:1].[ClH:1].[C:2]([NH:5][CH2:6][C:7]1[N:12]=[C:11]([C:13]2[N:14]=[C:15]([N:18]=[C:19]([NH2:20])[NH2:21])[S:16][CH:17]=2)[CH:10]=[CH:9][CH:8]=1)(=[O:4])[CH3:3]

Komponenten

5

Edukt 3

HCID 313Hydrochloric AcidHCID 7914Diisopropyl EtherHCID 104469404-(6-(Acetamidomethyl)pyridin-2-yl)-2-guanidinothiazole

Produkt 1

HCID 189538284-(6-Acetylaminomethylpyridin-2-yl)-2-(diaminomethyleneamino)thiazole dihydrochloride

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

4N-Dioxanic hydrogen chloride (48.0 ml) was added dropwise to a solution of 4-(6-acetylaminomethylpyridin-2-yl)-2-(diaminomethyleneamino)thiazole (18.6 g) in methanol (50 ml) at ambient temperature for 5 minutes. After the mixture was stirred at the same temperature for 30 minutes. To the mixture was added a diisopropyl ether and the isolated precipitate was collected by filtration. The precipitate was recrystallized from a mixture of methanol and diisopropyl ether to give 4-(6-acetylaminomethylpyridin-2-yl)-2-(diaminomethyleneamino)thiazole dihydrochloride (16.29 g).

Aufarbeitung

  1. filtrationthe isolated precipitate was collected by filtration
  2. customThe precipitate was recrystallized from a mixture of methanol and diisopropyl ether

Quellen und Nachweise

ORD-Eintrag
ord-4f8a4d56f670470d83da87686e22c464
Quelldatensatz
uspto-grants-1994_11
Patentnummer
US05364871

Notizen zur Reaktion

Wird geladen…