Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | HCID 86624609 | HCID 86624609 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 68778583 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07851634B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-8f500bc9630d4a54b2643941c8e5d194 |
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| Source note | uspto-grants-2010_12 |
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