HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Methane → 5-Chloro-2-[(2-methylphenyl)methyl]-1H-benzimidazole-6-sulfonamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Methane | HCID 297 | — |
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 2-(o-Tolyl)acetonitrile | HCID 31155 | — |
| Edukt | 4,5-Diamino-2-chlorobenzene-1-sulfonamide | HCID 13289688 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 5-Chloro-2-[(2-methylphenyl)methyl]-1H-benzimidazole-6-sulfonamide | HCID 13289710 | — |
Reaktionsschritte
To 50 ml of 6 N hydrochloric acid was added 11.8 g of 2-amino-4-chloro-5-sulfamylaniline and 10.4 g of 2-methylbenzyl cyanide. The reaction was refluxed for 22 hours and then concentrated in vacuo to a solid which was then added with stirring to 200 ml of 38% ammonium hydroxide. Filtration provided the free base as a semi-gum which was dissolved in 500 ml of methanol. The methanol solution was brought to a boil, charcoal added, and boiling continued for five minutes. Upon cooling, the suspension was filtered through Celite and the filtrate concentrated in vacuo to yield a solid, m.p. 226°-230°.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04420487 |
| Quelldatensatz | uspto-grants-1983_12 |
| ORD ID | ord-cb0c1604acbf44a68236af1dde3cf798 |
| Quellennotiz | uspto-grants-1983_12 |