HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528986Generated: October 29, 2026
Tetrabutylammonium Fluoride → HCID 86718932, compound
https://huagongshe.com/reaction/528986
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 71062635 | HCID 71062635 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86718932 | HCID 86718932 | 64.4% |
Reaction Steps
To a solution of ethyl 4-(4-(tert-butoxycarbonyl)-2-((S)-3-((tert-butyldimethylsilyloxy)methyl)-1,2,3,4-tetrahydroisoquinoline-2-carbonyl)phenyl)-5-butyl-1-phenyl-1H-pyrazole-3-carboxylate (Intermediate 259E, 207 mg, 0.275 mmol) in THF (2.0 mL) at room temperature was added TBAF (0.413 mL, 0.413 mmol). After stirring at room temperature for 1 h, the reaction mixture was diluted with EtOAc, washed with sat. aq. sodium bicarbonate solution, dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by flash chromatography (Isco 40 g column eluting with 0-70% EtOAc/hexanes) to give ethyl 4-(4-(tert-butoxycarbonyl)-2-((S)-3-(hydroxymethyl)-1,2,3,4-tetrahydroisoquinoline-2-carbonyl)phenyl)-5-butyl-1-phenyl-1H-pyrazole-3-carboxylate (113 mg, 0.177 mmol, 64%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09346795B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-e65f4413284f48dabc48e95bfe3b42fc |
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| Source note | uspto-grants-2016_05 |
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