HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 15614722, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Furoic acid | HCID 10268 | — |
| Reactant | 2-Chloro-1-methylpyridinium iodide | HCID 167069 | — |
| Reactant | HCID 13588033 | HCID 13588033 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15614722 | HCID 15614722 | 74% |
Reaction Steps
To a stirred mixture of 3.14 parts of 3-furancarboxylic acid, 6 parts of N,N-diethylethanamine and 390 parts of dichloromethane were added 7.2 parts of 2-chloro-1-methylpyridinium iodide. After stirring for 10 minutes at room temperature, 7 parts of 4-[(1H-benzimidazol-2-yl)amino]-1-piperidineacetonitrile were added and the whole was stirred for 1 hour at room temperature. The reaction mixture was washed with water. The organic phase was dried, filtered and evaporated. The residue was crystallized from acetonitrile, yielding 7 parts (74%) of 4-[[1-(3-furanylcarbonyl)-1H-benzimidazol-2-yl]amino]-1-piperidineacetonitrile (intermediate 101).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04820822 |
| Source dataset | uspto-grants-1989_04 |
| ORD ID | ord-274c8b1f723c449794418ff1d0888f24 |
| Source note | uspto-grants-1989_04 |