Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Guanidine Nitrate | HCID 10481 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 2-Chloro-5-(4-nitrophenyl)-1,3,4-thiadiazole | HCID 10514277 | — |
| Edukt | HCID 178418361 | HCID 178418361 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | HCID 178512737 | HCID 178512737 | 55% |
Reaktionsschritte
24.13 gm of guanidine nitrate were added in small portions over a period of 30 minutes to 6.5 gm of a 50% sodium hydride oil dispersion in 200 ml of dimethylformamide. After the evolution of hydrogen has ceased, a solution 15.8 gm of 2-chloro-5-(4-nitro-phenyl)-1,3,4-thiadiazole in 300 ml of dimethylformamide was added dropwise to the mixture, which was then stirred at room temperature for 2 hours, and then at 90° C. for 30 minutes. After cooling and dilution with water, the precipitate formed thereby was filtered off and dissolved in ethanol. Hydrogen chloride was added to this solution, and the hydrochloride which separated out was filtered off and dissolved in water, and the aqueous solution was made alkaline with 10% sodium hydroxide. The free base was filtered off, washed with water and dried, yielding 9.5 gm of the title compound, m.p. 295°-297° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04645841 |
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| Quelldatensatz | uspto-grants-1987_02 |
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| ORD ID | ord-b1130618595f4ea0bf6f0c74b22af9cf |
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| Quellennotiz | uspto-grants-1987_02 |
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