4-Methyl-3-oxopentanal → 2-Benzylthio-2-benzylthio-5-isopropyl-1,2,4-triazolo[1,5-a]pyrimidine

HRID 477220

Reaktionsgleichung

Reaktionsgleichung von HRID 477220
[NH2:1][C:2]1[N:6]=[C:5]([S:7][CH2:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[NH:4][N:3]=1.[CH3:15][CH:16]([CH3:22])[C:17](=O)[CH2:18][CH:19]=O>>[CH2:8]([S:7][C:5]1([S:7][CH2:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[N:6]=[C:2]2[N:1]=[C:17]([CH:16]([CH3:22])[CH3:15])[CH:18]=[CH:19][N:3]2[NH:4]1)[C:9]1[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=1

Komponenten

3

Edukt 2

HCID 147862684-Methyl-3-oxopentanalHCID 178509291HCID 178509291, Verbindung

Produkt 1

HCID 198373732-Benzylthio-2-benzylthio-5-isopropyl-1,2,4-triazolo[1,5-a]pyrimidineAusbeute 96 %

Versuchsvorschrift

This material was prepared in 96% yield from 3-amino-5-benzylthio-1,2,4-triazole and 4-methyl-3-oxopentanal following the general procedure described in Example 7. The desired product was isolated as a solid, m.p. 65°-66° C. IR and 1H NMR were in agreement with the assigned structure.

Quellen und Nachweise

ORD-Eintrag
ord-22ff46e77d9043b5808adaebdf58274d
Quelldatensatz
uspto-grants-1989_12
Patentnummer
US04886883

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