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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2163477Erstellt: 25. Oktober 2026

Dimethylformamide → 7-Thia-2,4,5-triazatricyclo(6.4.0.0,2,6)dodeca-1(12),3,5,8,10-pentaene

https://huagongshe.com/reaction/2163477

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktHydrazinecarboxaldehydeHCID 12229—
EduktSodium hydrideHCID 24758—
Edukt1-Chloro-2-isothiocyanatobenzeneHCID 123171—
LösungsmittelWaterHCID 962—
Produkt7-Thia-2,4,5-triazatricyclo(6.4.0.0,2,6)dodeca-1(12),3,5,8,10-pentaeneHCID 254568—

Reaktionsbedingungen

Temperatur160 °C

Reaktionsschritte

Five grams (30.0 mmoles) of o-chlorophenylisothiocyanate were dissolved in 50 ml. of dry DMF. A solution of 1.8 g. (30.0 mmoles) of formylhydrazine in 50 ml. of dry DMF was added dropwise rapidly to the stirred reaction mixture. The temperature of the reaction rose to about 45° C. The temperature was maintained between 60° C. and 100° C. for 24 hours. Thirty millimoles, 1.5 g., of sodium hydride as a 50% mineral oil suspension was added to the reaction mixture. The reaction was completed by heating at reflux temperature (160° C.) for about 185 hours. The cooled mixture was poured into water. The aqueous mixture was extracted with n-hexane to remove mineral oil. The product was extracted with ethyl acetate. The ethyl acetate extract was washed (water), dried (MgSO4) and evaporated in vacuo to a residual oil. The oil was covered with dry ether and the product crystallized upon standing. The yield of s-triazolo[3,4-b]benzothiazole, m.p. about 175-176° C., was 200 mg.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04134914
Quelldatensatzuspto-grants-1979_01
ORD IDord-bec31f8dc9fd4cbea289972bb9d6ad31
Quellennotizuspto-grants-1979_01