HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-[(Benzo-1,4-dioxan-2-yl)-methyl]-4-(6-chlorobenzimidazol-2-on-1-yl)-piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium cyanate | HCID 11378442 | — |
| Reactant | 1-[(Benzo-1,4-dioxan-2-yl)-methyl]-4-(5-chloro-2-aminoanilino)-piperidine | HCID 20446704 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-[(Benzo-1,4-dioxan-2-yl)-methyl]-4-(6-chlorobenzimidazol-2-on-1-yl)-piperidine | HCID 13792148 | — |
Reaction Steps
A solution of 4.8 g of potassium cyanate in 10 ml of water was added to 14.5 g of 1-[(benzo-1,4-dioxan-2-yl)-methyl]-4-(5-chloro-2-aminoanilino)-piperidine in 5 ml of 10% strength hydrochloric acid and 40 ml of water, whilst cooling and stirring. When the addition had ended, the mixture was stirred at room temperature for 1 hour and then under reflux for 24 hours. After the mixture had been cooled, it was extracted with chloroform. The extract was washed with 5% strength hydrochloric acid, dried and filtered and the filtrate was concentrated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04470989 |
| Source dataset | uspto-grants-1984_09 |
| ORD ID | ord-0bcc7aea091e4a83829f19bafffdda90 |
| Source note | uspto-grants-1984_09 |