HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719121Generated: November 1, 2026
Acetic Acid → 5-t-butoxycarbonylmethyl-3-(1-ethoxycarbonylethylamino)-2,3-dihydro-1,5-benzothiazepin-4(5H)-one
https://huagongshe.com/reaction/1719121
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethyl pyruvate | HCID 12041 | — |
| Reactant | 3-amino-5-t-butoxycarbonylmethyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one | HCID 13454542 | — |
| Reactant | Sodium boron cyanide hydride | HCID 131714321 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-t-butoxycarbonylmethyl-3-(1-ethoxycarbonylethylamino)-2,3-dihydro-1,5-benzothiazepin-4(5H)-one | HCID 13470779 | 50.3% |
Reaction Steps
1.5 g of 3-amino-5-t-butoxycarbonylmethyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one and 2.0 g of ethyl pyruvate were dissolved in 15 ml of ethanol. After the addition of 0.3 ml of acetic acid, the resulting mixture was stirred for 2 hours. Then, a solution of 420 mg of sodium boron cyanide hydride in 8 ml of ethanol was slowly added dropwise thereto. After this mixture was allowed to stand overnight, the solvent was distilled off under reduced pressure and the residue was dissolved in ethyl acetate. The resulting solution was washed with water, dried and then concentrated. The residue was purified by silica gel column chromatography using a 3:1 mixture of benzene and ethyl acetate as the eluent. Thus, there was obtained 1.0 g of the desired compound in the form of an oily material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04539150 |
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| Source dataset | uspto-grants-1985_09 |
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| ORD ID | ord-ba28893f3ca540019988b35937d0af92 |
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| Source note | uspto-grants-1985_09 |
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