Methane → (RS)-7-[(Pyrid-3-yl)imino]-4,4a,5,9-tetrahydrothiazolo[3,4-a]thieno[3,2-d]pyridine
Reaktionsgleichung
O[CH2:2][CH:3]1[N:8]([C:9](=[S:17])[NH:10][C:11]2[CH:12]=[N:13][CH:14]=[CH:15][CH:16]=2)[CH2:7][C:6]2[S:18][CH:19]=[CH:20][C:5]=2[CH2:4]1.C>Cl>[N:13]1[CH:14]=[CH:15][CH:16]=[C:11]([N:10]=[C:9]2[N:8]3[CH2:7][C:6]4[S:18][CH:19]=[CH:20][C:5]=4[CH2:4][CH:3]3[CH2:2][S:17]2)[CH:12]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A suspension of (RS)-5-hydroxymethyl-6-[(pyrid-3-yl)thiocarbamoyl]-4,5,6,7-tetrahydrothieno[2,3-c]pyridine (2.3 g) in 6 N hydrochloric acid (34 cc) is heated under reflux for 2 hours. The resulting brown solution is decolorised with animal charcoal and filtered. The filtrate is rendered alkaline to pH 11 with a 15% aqueous solution of potassium carbonate and extracted with methylene chloride (150 cc and then 3×100 cc). The organic extracts are combined and dried over sodium sulphate. After filtering and concentrating the filtrate to dryness under reduced pressure (25 mm Hg; 3.3 kPa) at 40° C., an oil is obtained which crystallises slowly. This oil is dissolved in a mixture, heated under reflux, of isopropanol and diisopropyl ether (4:1 by volume; 100 cc). The solution is cooled at +5° C. for 20 hours. The solid is filtered off, washed with diisopropyl ether (50 cc) and dried at 60° C. under reduced pressure (0.1 mm Hg; 0.013 kPa). (RS)-7-[(Pyrid-3-yl)imino]-4,4a,5,9-tetrahydrothiazolo[ 3,4-a]thieno[3,2-d]pyridine (1.2 g) is obtained in the form of white crystals melting at 136° C.