HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzimidazole → 1-{4-[4-(2-pyrimidinyl)-1-piperazinyl]butyl}-1H-benzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzimidazole | HCID 5798 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(4-(4-Bromobutyl)piperazin-1-yl)pyrimidine | HCID 14726843 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-{4-[4-(2-pyrimidinyl)-1-piperazinyl]butyl}-1H-benzimidazole | HCID 9819148 | — |
Reaction Steps
A mixture of 6 g (20 mmol) of 2-[4-(4-bromobutyl)-1-piperazinyl]-pyrimidine, 2.36 g (20 mmol) of benzimidazole and 4.1 g (30 mmol) of potassium carbonate in 60 ml of dimethylformamide is refluxed for 14 hours. The reaction mixture is evaporated under vacuum, chloroform is added, the mixture is washed with water, dried over sodium sulphate and evaporated under vacuum and 4.8 g of 1-{4-[4-(2-pyrimidinyl)-1-piperazinyl]-butyl}-1H-benzimidazole are obtained, which may be recrystallised from ethyl ether, with a melting point of 85°-88° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05382586 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-bb9f9015a0814603b73a671f894d6868 |
| Source note | uspto-grants-1995_01 |