HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 10026551, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | HCID 18631458 | HCID 18631458 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 10026551 | HCID 10026551 | 76.1% |
Reaction Steps
In 8 ml of 1N aqueous sodium hydroxide is dissolved 0.3 g of (S)-2-[N-[(S)-1-ethoxycarbonyl-5-(4-piperidyl)pentyl]-L-alanyl]-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid.dihydrobromide, and the solution is allowed to stand at room temperature for 1 hour. The reaction solution is made acidic with 1 ml of acetic acid, and then purified by Amberlite XAD-2 column chromatography (0.1M aqueous ammonia-5% acetonitrile). The effluent is concentrated under reduced pressure, and lyophilized to give 0.16 g of (S)-2-[N-[(S)-1-carboxy-5-(4-piperidyl)pentyl]-L-alanyl]-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid as a colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04954625 |
| Source dataset | uspto-grants-1990_09 |
| ORD ID | ord-437aa0b38d424c2d97c0f58cc4833a52 |
| Source note | uspto-grants-1990_09 |