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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351213Generated: October 29, 2026

Sodium Acetate → HCID 11765114, compound

https://huagongshe.com/reaction/2351213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantEthyl 6-(1-benzyloxycarbonyl-4-piperidyl)-2-oxohexanoateHCID 13817563—
ReactantHCID 86743426HCID 86743426—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
ProductHCID 11765114HCID 1176511410.5%

Reaction Steps

A solution of 0.6 g of sodium cyanoborohydride in 50 ml of ethanol is added dropwise to a stirred mixture of 2 g of N-(L-alanyl)-N-(2-indanyl)glycine tert-butyl ester·oxalate, 0.78 g of sodium acetate, 0.58 g of acetic acid, 10 g of molecular sieves 3A, 3.6 g of ethyl 6-(1-benzyloxycarbonyl-4-piperidyl)-2-oxohexanoate and 50 ml of ethanol at room temperature over a period of 3 hours. The reaction solution is allowed to stand overnight and filtered, and the filtrate is concentrated under reduced pressure. The residue is diluted with 50 ml of water and extracted with 200 ml of ethyl acetate. The extract is dried and concentrated under reduced pressure. The resulting oily material is separated and purified by silica gel column chromatography (hexane:ethyl acetate=1:1 to 2:3), whereby the first fraction yields 0.35 g of N-[N-[(R)-5-(1-benzyloxycarbonyl-4-piperidyl)-1-ethoxycarbonylpentyl]-L-alanyl]-N-(indan-2-yl)glycine tert-butyl ester as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04871842
Source datasetuspto-grants-1989_10
ORD IDord-4cac8bf6aa084f1988bc79b6867c6540
Source noteuspto-grants-1989_10