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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthyl pyruvateHCID 12041—
Reactant3-amino-5-t-butoxycarbonylmethyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-oneHCID 13454542—
ReactantSodium boron cyanide hydrideHCID 131714321—
SolventEthanolHCID 702—
Product5-t-butoxycarbonylmethyl-3-(1-ethoxycarbonylethylamino)-2,3-dihydro-1,5-benzothiazepin-4(5H)-oneHCID 1347077950.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04539150
Source datasetuspto-grants-1985_09
ORD IDord-ba28893f3ca540019988b35937d0af92
Source noteuspto-grants-1985_09