HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 10253690, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | HCID 18631455 | HCID 18631455 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 10253690 | HCID 10253690 | 62.2% |
Reaction Steps
In 6 ml of 1N aqueous sodium hydroxide is dissolved 0.25 g of N-[N-[(S)-1-ethoxycarbonyl-5-(4-piperidyl)pentyl]-L-alanyl]-N-(indan-2-yl)glycine.dihydrobromide, and the solution is allowed to stand at room temperature for 30 minutes. The reaction is made weakly acidic with acetic acid and purified by column chromatography on Amberlite XAD-2 (0.1M aqueous ammonia-5% acetonitrile). The effluent is concentrated under reduced pressure and lyophilized to give 0.11 g of N-[N-[(S)-1-carboxy-5-(4-piperidyl)pentyl]-L-alanyl]-N-(indan-2-yl)glycine as a colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04816466 |
| Source dataset | uspto-grants-1989_03 |
| ORD ID | ord-d2228ed0ba9f4e52b54696132393fa91 |
| Source note | uspto-grants-1989_03 |