HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 70416336, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Acetic Acid Mixture with Hydrobromic Acid | HCID 21893785 | — |
| Reactant | HCID 54311947 | HCID 54311947 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 70416336 | HCID 70416336 | — |
Reaction Steps
In 1 ml of acetic acid is dissolved 0.45 g of tert-butyl 3(R)-[5-(1-benzoyloxycarbonyl-4-piperidyl)-1(R)-ethoxycarbonylpentyl]amino-4-oxo-2,3,4,5-tetrahydro-1,5-benzothiazepine-5-acetate, and 1 ml of 30% hydrogen bromide-acetic acid solution is added to the solution, followed by allowing the mixture to stand at room temperature for 1.5 hours. Ethyl ether (200 ml) is added to the reaction solution, which is then allowed to stand. The supernatant liquid is decanted, and the precipitate is washed with ethyl ether and dried to give 0.3 g of 3(R)-[1(R)-ethoxycarbonyl-5-(4-piperidyl)pentyl]amino-4-oxo-2,3,4,5-tetrahydro-1,5-benzothiazepin-5-acetic acid.dihydrobromide 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-41b9ec5078254ab5b990041eaa504a2f |
| Source note | uspto-grants-1988_04 |