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HRID 2163477作成日:2026年10月26日

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

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物HydrazinecarboxaldehydeHCID 12229—
反応物Sodium hydrideHCID 24758—
反応物1-Chloro-2-isothiocyanatobenzeneHCID 123171—
溶媒WaterHCID 962—
生成物7-Thia-2,4,5-triazatricyclo(6.4.0.0,2,6)dodeca-1(12),3,5,8,10-pentaeneHCID 254568—

反応条件

温度160 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04134914
出典データセットuspto-grants-1979_01
ORD IDord-bec31f8dc9fd4cbea289972bb9d6ad31
出典メモuspto-grants-1979_01