HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464873Generated: October 30, 2026
Acetic Acid Mixture with Hydrobromic Acid → HCID 53889850, compound
https://huagongshe.com/reaction/464873
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid Mixture with Hydrobromic Acid | HCID 21893785 | — |
| Reactant | HCID 54149894 | HCID 54149894 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 53889850 | HCID 53889850 | 68.4% |
Reaction Steps
To a solution of tert-butyl 3(S)-[6-(1-benzyloxycarbonyl-4-piperidyl)-1(S)-ethoxycarbonylhexyl]amino-4-oxo-2,3,4,5-tetrahydro-1,5-benzoxazepine-5-acetate (0.5 g) in acetic acid (1 ml) is added 30% hydrogen bromide-acetic acid solution (2 ml). The resulting mixture is allowed to stand for 1 hour at room temperature and then diluted with ethyl ether (100 ml). The supernatant layer is removed by decantation and the precipitate is dissolved in 1N sodium hydroxide solution (20 ml). The solution is allowed to stand for 30 minutes at room temperature. After addition of acetic acid (4 ml), the mixture is chromatographed on MCI gel using water-methanol (1:2) as an eluent. The eluate is concentrated in vacuo and lyophilized to give 3(S)-[1(S)-carboxy-6-(4-piperidyl)hexyl]amino-4-oxo-2,3,4,5-tetrahydro-1,5-benzoxazepine-5-acetic acid (0.23 g) as colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04548932 |
|---|
| Source dataset | uspto-grants-1985_10 |
|---|
| ORD ID | ord-8ed5c8926f284ad599ae8d0acb8a6d43 |
|---|
| Source note | uspto-grants-1985_10 |
|---|