HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459535Generated: October 30, 2026
Tetrabutylammonium Fluoride → HCID 58822274, compound
https://huagongshe.com/reaction/459535
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 57864676 | HCID 57864676 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58822274 | HCID 58822274 | 67.5% |
Reaction Steps
(1S,2S,4R)-N1-tert-Butoxycarbonyl-4-(tert-butyldiphenylsilyloxymethyl)-N2-[(5-methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridin-2-yl)carbonyl]-1,2-cyclohexanediamine (1.25 g) was dissolved in tetrahydrofuran (30 ml), and tetrabutylammonium fluoride (1 M solution, 2.5 ml), and the mixture was stirred at room temperature for 3 days. After the solvent was distilled off under reduced pressure, dichloromethane was added, and the reaction mixture was washed with water, the resultant organic layer was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by column chromatography on silica gel (methanol:dichloromethane=1:20-1:10) to obtain the title compound (540 mg) as a pale yellow amorphous substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07192968B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-19b2cb3c49b24ed9a604bb19c83390ea |
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| Source note | uspto-grants-2007_03 |
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