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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2163477Generated: October 25, 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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantHydrazinecarboxaldehydeHCID 12229—
ReactantSodium hydrideHCID 24758—
Reactant1-Chloro-2-isothiocyanatobenzeneHCID 123171—
SolventWaterHCID 962—
Product7-Thia-2,4,5-triazatricyclo(6.4.0.0,2,6)dodeca-1(12),3,5,8,10-pentaeneHCID 254568—

Reaction Conditions

Temperature160 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04134914
Source datasetuspto-grants-1979_01
ORD IDord-bec31f8dc9fd4cbea289972bb9d6ad31
Source noteuspto-grants-1979_01