HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477674Generated: November 2, 2026
Trifluoroacetic acid → HCID 136933045, compound
https://huagongshe.com/reaction/1477674
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 117839254 | HCID 117839254 | — |
| Reactant | HCID 117839615 | HCID 117839615 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 136933045 | HCID 136933045 | 94% |
Reaction Steps
To 1-(4-methoxybenzyl)-6-methyl-4-(methylthio)-1,3,5-triazin-2(1H)-one (1.39 g, 5.0 mmol) synthesized in Reference Synthesis Example 315, trifluoroacetic acid (10 mL) was added and the resultant mixture was stirred for 1 hour under reflux. After completion of the reaction, the reaction solution was concentrated under reduced pressure and 1,4-dioxane (10 mL), (R)-4-(4-fluorophenyl)-1,2,3,6-tetrahydropyridin-3-ol (966 mg, 5.00 mmol) synthesized in Reference Synthesis Example 133, and N,N-diisopropylethylamine (1.92 g, 10.0 mmol) were added to the concentrated solution, followed by refluxing the resultant mixture for 2 hours. After completion of the reaction, water was added to the reaction solution and extraction from the resultant mixture with ethyl acetate was performed. The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl acetate/methanol=10/1) to obtain the title compound (1.41 g, yield 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09403798B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-3e4bfc40dd2840d2a0f3dda37410cb75 |
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| Source note | uspto-grants-2016_08 |
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