HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503072Generated: October 30, 2026
Trifluoroacetic acid → HCID 86722597, compound
https://huagongshe.com/reaction/1503072
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | HCID 86722598 | HCID 86722598 | — |
| Reactant | HCID 178484293 | HCID 178484293 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86722597 | HCID 86722597 | — |
Reaction Steps
To a solution of (E)-N-(2-amino-2-methylpropyl)-4-(4,4,4-trifluoro-3-(3,4,5-trichlorophenyl)but-1-en-1-yl)-2-(trifluoromethyl)benzamide (155 mg, 0.283 mmol), 1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium 3-oxid hexafluorophosphate (HATU) (118 mg, 0.311 mmol), and 2,2,2-trifluoroacetic acid (0.026 mL, 0.340 mmol) in DMF (1 mL) was—added N-methylmorpholine (0.062 mL, 0.566 mmol). The mixture was stirred at ambient temperature for 18 h, —then partitioned between water and EtOAc. The organic phase was washed with water and—brine, —dried (sodium sulfate) and concentrated—under reduced pressure. Purification by column chromatography eluting with EtOAc in hexanes (10%-100%)—afforded the title compound as a yellow oil (26 mg, 13%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09211281B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-c477bc0342384e3d814b47d07b71d2f8 |
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| Source note | uspto-grants-2015_12 |
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