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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980592Generated: October 29, 2026

Glutaraldehyde → HCID 70416287, compound

https://huagongshe.com/reaction/980592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlutaraldehydeHCID 3485—
ReactantSodium ChlorideHCID 5234—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 70416887HCID 70416887—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 70416287HCID 70416287147%

Reaction Steps

In 5 ml of ethanol is dissolved 60 mg of ethyl 3(R)-(5-amino-1-ethoxycarbonylpentyl)amino-4-oxo-2,3,4,5-tetrahydro-1,5-benzothiazepine-5-acetate dihydrochloride, and 0.5 g of 25% aqueous glutaraldehyde solution and 0.3 g of sodium cyanoborohydride are added to the solution, followed by stirring at room temperature for 2 hours. Water (50 ml) is added to the reaction solution, followed by adding sodium chloride to saturate the solution. The solution is extracted twice with 30 ml of ethyl acetate, and the extract is washed with water, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting oily material is dissolved in a small amount of ethyl ether, and 0.2 ml of 5N hydrogen chloride-ethyl acetate solution is added to the solution to give 50 mg of ethyl 3(R)-(1-ethoxycarbonyl-5-piperidinopentyl)amino-4-oxo-2,3,4,5-tetrahydro-1,5-benzothiazepine-5-acetate.dihydrochloride as a colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04638000
Source datasetuspto-grants-1987_01
ORD IDord-66cb9ec07e18441d9443f3c7a7157448
Source noteuspto-grants-1987_01