HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → p-Chlorophenyl 1-amidino-4-piperidinecarboxylate hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Bis-(p-chlorophenyl)sulfite | HCID 20449815 | — |
| Reactant | 1-Amidino-4-piperidinecarboxylic acid hydrochloride | HCID 70043897 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | p-Chlorophenyl 1-amidino-4-piperidinecarboxylate hydrochloride | HCID 20470413 | 70.5% |
Reaction Steps
A mixture of 1.5 g of 1-amidino-4-piperidinecarboxylic acid hydrochloride and 8.8 g of bis-(p-chlorophenyl)sulfite was stirred at room temperature for 1 hour in a solution of 14 ml of dry dimethylformamide and 7 ml of dry pyridine. The solvent was removed under reduced pressure, and the residue was washed twice with dry ether. Acetone was added to the residue to give crystals. The crystals were washed with ether and then with ethyl acetate and recrystallized from methanol-ether to obtain 1.62 g (yield: 70.4%) of p-chlorophenyl 1-amidino-4-piperidinecarboxylate hydrochloride as colorless crystals having a melting point of 196° to 198° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04433152 |
| Source dataset | uspto-grants-1984_02 |
| ORD ID | ord-3006300221724cdba5c1c591ffadd2f9 |
| Source note | uspto-grants-1984_02 |