Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Urea | HCID 1176 | — |
| Reactant | HCID 70611928 | HCID 70611928 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 20379499 | HCID 20379499 | 63.5% |
Reaction Steps
A mixture of 41.5 parts of 4-chloro-N1 -[1-(3-pyridinyl)ethyl]-1,2-benzenediamine monohydrochloride and 27 parts of urea is stirred and heated for 1.50 hours in an oil-bath at about 190° C. The reaction mixture is cooled, water and trichloromethane are added and the layers are separated. The organic phase is dried, filtered and evaporated. The residue is crystallized from a mixture of 4-methyl-2-pentanone and 2,2'-oxybispropane. The product is filtered off and dried, yielding 26 parts (63.5%) of 5-chloro-1,3-dihydro-1-[1-(3-pyridinyl)ethyl]-2H-benzimidazol-2-one; mp. 190° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04181802 |
|---|
| Source dataset | uspto-grants-1980_01 |
|---|
| ORD ID | ord-cd21ca143bca4a98bcb583afcd719697 |
|---|
| Source note | uspto-grants-1980_01 |
|---|