HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536761Generated: October 31, 2026
Methyl triflate → HCID 178480273, compound
https://huagongshe.com/reaction/536761
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl triflate | HCID 9526 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | n-[3-Tert-butyl-1-(4,4,4-trifluorobutyl)-1h-pyrazol-5-yl]-2-fluoro-5-(trifluoromethyl)benzamide | HCID 87087570 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178480273 | HCID 178480273 | 74.4% |
Reaction Steps
To a solution of Example 135C (1.7 g, 3.9 mmol) in toluene (15 mL) was added methyl trifluoromethanesulfonate (0.64 mL, 5.8 mmol). The mixture was warmed to 100° C. and stirred for 20 hours, cooled to ambient temperature and diluted with water (20 mL) and acetone (50 mL). This solution was allowed to stir for 30 minutes then concentrated NH4OH (10 mL) was added. The mixture was stirred for 30 minutes then partially concentrated under reduced pressure. The mixture was diluted with EtOAc (30 mL) and brine (10 mL) and the layers were separated. The aqueous phase was extracted with EtOAc (3×5 mL). The combined organic extracts were dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. Purification by column chromatography (SiO2, 80% hexanes/EtOAc to 100% EtOAc to 10% MeOH in EtOAc) afforded the title compound (1.3 g, 2.9 mmol, 74% yield). MS (ESI+) m/z 454 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859596B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-5fcf102ff54c4ff1b99fc8c778dc19aa |
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| Source note | uspto-grants-2014_10 |
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