HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20239Generated: October 28, 2026
Tetrabutylammonium Fluoride → HCID 59347369, compound
https://huagongshe.com/reaction/20239
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 59347365 | HCID 59347365 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59347369 | HCID 59347369 | 54% |
Reaction Steps
Tetrabutylammonium fluoride (0.12 g) was added to a solution of 1-(2-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-3-(1-{(2S)-3-[(6-chloronaphthalen-2-yl)sulfonyl]-2-hydroxypropanoyl}piperidin-4-yl)tetrahydropyrimidin-2(1H)-one (0.25 g) obtained in Example 40c) in THF (10 mL), and the mixture was stirred at room temperature overnight. The solvent was distilled off under reduced pressure, and the residue was diluted with ethyl acetate. The mixture was washed with an aqueous 5% citric acid solution and saturated saline solution, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (ethyl acetate/methanol=95/5 to ethyl acetate/methanol=90/10) to obtain the title compound (0.11 g, 54%) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07745623B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-fee37a8f060a46adaea03959847f94d9 |
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| Source note | uspto-grants-2010_06 |
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