HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 1-[3-{4-[(2-chlorophenyl)phenylmethyl]-1-piperazinyl}propyl]1H-benzimidazole trihydrochloride dihydrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1-(3-Chloropropyl)-1H-benzimidazole | HCID 13105517 | — |
| Reactant | 1-[(2-Chlorophenyl)phenylmethyl]piperazine acetate | HCID 70534570 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | 1-[3-{4-[(2-chlorophenyl)phenylmethyl]-1-piperazinyl}propyl]1H-benzimidazole trihydrochloride dihydrate | HCID 70535024 | — |
Reaction Steps
A mixture of 4.9 parts of 1-(3-chloropropyl)-1H-benzimidazole, 7 parts of 1-[(2-chlorophenyl)phenylmethyl]piperazine acetate, 10.6 parts of sodium carbonate, 0.1 parts of potassium iodide and 200 parts of 4-methyl-2-pentanone is stirred and refluxed for 20 hours with water-separator. The reaction mixture is cooled, water is added and the layers are separated. The organic phase is dried, filtered and evaporated. The residue is converted into the hydrochloride salt in 2-propanol and 2,2'-oxybispropane. The salt is filtered off and crystallized from 2-propanol, yielding 1-[3-{4-[(2-chlorophenyl)phenylmethyl]-1-piperazinyl}propyl]-1H-benzimidazole trihydrochloride dihydrate; mp. 182.9° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04377578 |
| Source dataset | uspto-grants-1983_03 |
| ORD ID | ord-6d4cde76017b4b41a0b9325c0fc55f59 |
| Source note | uspto-grants-1983_03 |