HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Piperidinecarboxamide → benzyl 4-(aminocarbonyl)tetrahydro-1(2H)-pyridinecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Piperidinecarboxamide | HCID 3772 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | benzyl 4-(aminocarbonyl)tetrahydro-1(2H)-pyridinecarboxylate | HCID 2776131 | 76% |
Reaction Steps
To a solution of piperidine-4-carboxamide (5 g, 39 mmol) and benzylchloroformate (5.54 mL, 39 mmol) in a mixture of water (30 mL) and acetone (40 mL), NaOH 1N (39 mL, 39 mmol) was added dropwise, while maintaining the pH between 6 and 8. The mixture was stirred at r.t. for 3 h; then acetone was evaporated and the resulting precipitate filtered and dried at 70° C. under reduced pressure, giving 7.75 g of benzyl-4-carbamoylpiperidine-1-carboxylate (76%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09199979B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-7d8dfbdbecc44e4f9aa4d905818ba5ff |
| Source note | uspto-grants-2015_12 |