HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Triethylamine → 2-(1H-Benzoimidazol-2-YL)-2H-[1,2,4]triazol-3-ylamine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 2-hydrazinyl-1H-1,3-benzodiazole | HCID 95788 | — |
| Edukt | Methanimidic acid, N-cyano-, ethyl ester | HCID 9920370 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 2-(1H-Benzoimidazol-2-YL)-2H-[1,2,4]triazol-3-ylamine | HCID 608264 | — |
Reaktionsbedingungen
| Temperatur | 0 °C |
|---|
Reaktionsschritte
To a solution of 2-hydrazino-1H-benzimidazole (5.0 g, 33.7 mmol) in ethanol (30 ml) is added sequentially triethylamine (5 ml, 33.7 mmol) and N-cyanoformimidic acid ethyl ester (3.3 g, 33.7 mmol) with cooling. After stirring for 2 hours at 0° C. the resulting precipitate is filtered with suction and dried to give 3-amino-2-(1H-benzimidazol-2-yl)-1,2,4-triazole. 1H-NMR (400 MHz, d6-DMSO): 13.0 (s, 1H); 7.77 (s,1H); 7.70 (m, 2H); 7.50 (m, 2H); 7.20 (s, 2H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07423157B2 |
| Quelldatensatz | uspto-grants-2008_09 |
| ORD ID | ord-7f10adc0d7e24d279472728a0b3b4fc5 |
| Quellennotiz | uspto-grants-2008_09 |