HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → 1-Methyl-5-nitro-1H-benzimidazol-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | 1-N-methyl-4-nitrobenzene-1,2-diamine | HCID 3420025 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Methyl-5-nitro-1H-benzimidazol-2-amine | HCID 45078636 | — |
Reaction Steps
To a solution of N1-methyl-4-nitro-benzene-1,2-diamine (200 mg, 1.20 mmol) in methanol (12 ml) was added cyanogen bromide (190.1 mg, 1.79 mmol). After stirring at room temperature for 16 h, the methanol was removed in vacuo and the resulting solid was stirred with diethyl ether (40 ml) for 5 minutes. The resulting hydrobromide salt of the title compound was filtered and air-dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07338959B2 |
| Source dataset | uspto-grants-2008_03 |
| ORD ID | ord-a44532fd00534422a86455a70c8c0659 |
| Source note | uspto-grants-2008_03 |