HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-{[4-(2-Tert-butylphenyl)piperazin-1-yl](oxo)acetyl}piperidine-4-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Methyl 1-{[4-(2-tert-butylphenyl)piperazin-1-yl](oxo)acetyl}piperidine-4-carboxylate | HCID 66751159 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-{[4-(2-Tert-butylphenyl)piperazin-1-yl](oxo)acetyl}piperidine-4-carboxylic acid | HCID 66751324 | 96% |
Reaction Steps
To a stirred solution of methyl 1-{[4-(2-tert-butylphenyl)piperazin-1-yl](oxo)acetyl}piperidine-4-carboxylate (Example 88, 0.159 g, 0.383 mmol) in THF (3 mL) stirring at 0° C. was added 1 M lithium hydroxide solution (3 mL, 3 mmol). After 2 h the reaction mixture was acidified with 1 M hydrochloric acid solution and extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO4, and the solvent was evaporated under reduced pressure to provide 1-{[4-(2-tert-butylphenyl)piperazin-1-yl](oxo)acetyl}piperidine-4-carboxylic acid (0.147 g, 96%) as a white amorphous.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08853215B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-0cd27e077c52466c80485f1caf7250c6 |
| Source note | uspto-grants-2014_10 |