HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → 5-chloro-1-(tetrahydro-pyran-4-ylmethyl)-1H-benzimidazol-2-ylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | 4-chloro-N1-(tetrahydro-pyran-4-ylmethyl)-benzene-1,2-diamine | HCID 63725955 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-chloro-1-(tetrahydro-pyran-4-ylmethyl)-1H-benzimidazol-2-ylamine | HCID 55227979 | — |
Reaction Steps
4-Chloro-N1-(tetrahydro-pyran-4-ylmethyl)-benzene-1,2-diamine (1.026 g; 4.261 mmol) is dissolved in ethanol (65 mL) and cyanogen bromide (0.903 g; 8.522 mmol) is added. The reaction is stirred at room temperature overnight. After this time the mixture is concentrated in vacuo to afford title compound as a tan solid which was used without further purification. ESI m/z 266 [M+H]+/264 [M−H]−
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08629157B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-3923116476e1420eac7938d38431a599 |
| Source note | uspto-grants-2014_01 |