HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 13652707, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | HCID 70416348 | HCID 70416348 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 13652707 | HCID 13652707 | 86.2% |
Reaction Steps
In 12 ml of 1N aqueous sodium hydroxide solution is dissolved 0.5 g of 3(R)-[1(S)-ethoxycarbonyl-4-(4-piperidyl)butyl]amino-4-oxo-2,3,4,5-tetrahydro-1,5-benzothiazepine-5-acetic acid.dihydrobromide, and the solution is allowed to stand at room temperature for 30 minutes. The solution is neutralized with 2 ml of acetic acid, and purified by MCI-gel (CHP 20P, 150 to 300μ, Mitsubishi Chemical Industries, Japan) column chormatography (water:methanol=2:1). The eluent is concentrated under reduced pressure, and the residue is lyophilized to give 0.3 g of 3(R)-[1(S)-carboxy-4-(4-piperidyl)butyl]amino-4-oxo-2,3,4,5-tetrahydro-1,5-benzothiazepine-5-acetic acid as a colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04739066 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-34d41b4901b34dc9a42c5d89d0df3034 |
| Source note | uspto-grants-1988_04 |