HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Chloro-1,3-dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-one → HCID 21428799, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Chloro-1,3-dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-one | HCID 104607 | — |
| Reactant | N-(2-Bromoethyl)-2-nitrobenzene-1-carboximidic acid | HCID 3017373 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21428799 | HCID 21428799 | 67% |
Reaction Steps
A mixture of 1.5 parts of N-(2-bromoethyl)-2-nitrobenzamide, 1.55 parts of 5-chloro-1,3-dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-one and 27 parts of N,N-dimethylformamide is stirred and refluxed for 5 hours. The reaction mixture is evaporated and the oily residue is crystallized from ethanol. The product is filtered off and dried, yielding 2.2 parts (67%) of N-{2-[4-(5-chloro-2,3-dihydro-2-oxo- 1H-benzimidazol-1-yl)-1-piperidinyl] ethyl}-2-nitrobenzamide hydrobromide. hemihydrate; mp. 273.2° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04031226 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-c3f6cfc090ed4d929007242e546b3cfe |
| Source note | uspto-grants-1977_06 |