HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → 2-Amino-5-(4-fluorophenylsulfonyloxy)benzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | Luxabendazole | HCID 72019 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Amino-5-(4-fluorophenylsulfonyloxy)benzimidazole | HCID 20221070 | — |
Reaction Steps
14.1 g of 1,2-diamino-4-(4-fluorophenylsulfonyloxy)benzene (see Example 1) and 5.8 g of cyanogen bromide in 150 ml of methanol are heated to reflux for 6 h, then the mixture is cooled and concentrated. The residue is dissolved in water, and ammonia is added with cooling. The precipitated 2-aminobenzimidazole derivative is filtered off with suction, washed with water, dried and recrystallized from ethyl acetate and diisopropyl ether, with the addition of active charcoal; melting point 192° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04639463 |
| Source dataset | uspto-grants-1987_01 |
| ORD ID | ord-a3055375963c48ff9048b61c08f3f684 |
| Source note | uspto-grants-1987_01 |