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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2263557Generated: November 3, 2026

Ethanolamine → HCID 68778583, compound

https://huagongshe.com/reaction/2263557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
ReactantHCID 86624609HCID 86624609—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 68778583HCID 68778583—

Reaction Steps

The stirred solution of 1.86 g of 2-[2 azido-2-(4-isopropyl-5-oxotetrahydrofuran-2-yl)ethyl]-1-[3-(3-methoxypropyl)-1-(2-trimethylsilanylethoxymethyl)-1H-indol-5-yl]-3-methylbutyl methoxyacetate (diastereomer mixture) in 100 ml of ethanol is hydrogenated at 0° C. in the presence of 0.165 ml of ethanolamine and 1.88 g of 10% Pd/C over 6 hours. The reaction mixture is clarified by filtration and the filtrate is concentrated by evaporation. The residue is admixed with 100 ml of 1M sodium hydrogencarbonate solution and extracted with tert-butyl methyl ether (3×). The combined organic phases are dried over sodium sulphate and filtered, and the filtrate is concentrated by evaporation. The crude title compound is obtained as a colourless oil from the residue by means of flash chromatography (SiO2 60 F). Rt=24.2 (gradient II).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851634B2
Source datasetuspto-grants-2010_12
ORD IDord-8f500bc9630d4a54b2643941c8e5d194
Source noteuspto-grants-2010_12