HuagongsheHuagongshe Chemistry Print Report · For research reference only
benzyl N-{[4-(2-tert-butylphenyl)piperazin-1-yl](oxo)acetyl}glycinate → N-{[4-(2-tert-butylphenyl)piperazin-1-yl](oxo)acetyl}glycine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | benzyl N-{[4-(2-tert-butylphenyl)piperazin-1-yl](oxo)acetyl}glycinate | HCID 66751166 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-{[4-(2-tert-butylphenyl)piperazin-1-yl](oxo)acetyl}glycine | HCID 66750891 | 98.2% |
Reaction Steps
A suspension of benzyl N-{[4-(2-tert-butylphenyl)piperazin-1-yl](oxo)acetyl}glycinate (Example 86, 350 mg, 0.80 mmol) and palladium hydroxide (20% on carbon, wetted with ca. 50% water, 30 mg) in ethyl acetate (25 mL) was stirred under hydrogen atmosphere at room temperature for 3 h. The reaction mixture was filtered and the filtrate was concentrated under reduced pressure to provide N-{[4-(2-tert-butylphenyl)piperazin-1-yl](oxo)acetyl}glycine (0.273 g, 98%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08853215B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-5f3657dd611d49928b1ba766a8430216 |
| Source note | uspto-grants-2014_10 |