HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284948Generated: October 31, 2026
HCID 70416343, compound → HCID 53869746, compound
https://huagongshe.com/reaction/1284948
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 70416343 | HCID 70416343 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 53869746 | HCID 53869746 | 85.8% |
Reaction Steps
Ethyl 3(R)-(5-benzyloxycarbonylamino-1-ethoxycarbonylpentyl)amino-4-oxo-2,3,4,5-tetrahydro-1,5-benzothiazepine-5-acetate hydrochloride (55 mg) obtained in Example 52-(1) is dissolved in a mixture of ethanol (3 ml) and 1N aqueous sodium hydroxide (2 ml). The solution is allowed to stand for 1 hour at room temperature, diluted with water (50 ml) and extracted with ethyl ether (20 ml). The aqueous layer is acidified to pH 4 with 1N hydrochloric acid, saturated with ammonium chloride and extracted ten times with ethyl acetate (20 ml each). The extract is washed with a small amount of water, dried over anhydrous magnesium sulfate and concentrated to dryness under reduced pressure to yield 3(R)-(5-benzyloxycarbonylamino-1-carboxypentyl)amino-4-oxo-2,3,4,5-tetrahydro-1,5-benzothiazepine-5-acetic acid (40 mg) as colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04564612 |
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| Source dataset | uspto-grants-1986_01 |
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| ORD ID | ord-2fb2b5dbc2ee4c41802b1d0ea0d5112c |
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| Source note | uspto-grants-1986_01 |
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