HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-t-Butyloxycarbonyl-4-((2-carboxymethoxyphenyl)amino)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 22380729 | HCID 22380729 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-t-Butyloxycarbonyl-4-((2-carboxymethoxyphenyl)amino)piperidine | HCID 22380704 | 75% |
Reaction Steps
1-(tert-Butoxycarbonyl)-4-[(2-methoxycarbonylmethoxyphenyl)amino]piperidine (100 mg) was dissolved in methanol (1 ml), added with 1 N aqueous sodium hydroxide (0.55 ml) and stirred at room temperature for 1 hour. The reaction mixture was neutralized with 1 N aqueous hydrochloric acid and extracted twice with ethyl acetate (3 ml). The organic layer was dried over anhydrous magnesium sulfate, and then the solvent was evaporated under reduced pressure to obtain 72.1 mg of the title compound. Yield: 75%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06916822B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-0827ad2a133c4dd1bdacd911f2caabe2 |
| Source note | uspto-grants-2005_07 |