HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587209Generated: October 29, 2026
Diisopropylethylamine → HCID 86675140, compound
https://huagongshe.com/reaction/587209
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | 3,3,3-Trifluoropropionic acid | HCID 2777972 | — |
| Reactant | HCID 86675137 | HCID 86675137 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86675140 | HCID 86675140 | — |
Reaction Steps
To a stirred solution of 3,3,3-trifluoropropanoic acid (0.02 g, 0.16 mmol) in CH2Cl2 (10.0 mL), (E)-2-bromo-N-(piperidin-4-yl)-4-(4,4,4-trifluoro-3-(3,4,5-trichlorophenyl)but-1-enyl)benzamide (0.1 g, 0.16 mmol), PYBOP (0.09 g, 0.17 mmol), and DIPEA (0.06 g, 0.48 mmol) were added at ambient temperature. The reaction mixture was stirred at ambient temperature for 5 h. The reaction mixture was diluted with CH2Cl2. The combined CH2Cl2 layer was washed with 3N HCl and saturated NaHCO3 solution, the separated CH2Cl2 layer was dried over anhydrous Na2SO4 and concentrated under reduced pressure to afford crude compound. The crude compound was purified by column chromatography (SiO2, 100-200 mesh; eluting with 2% MeOH in CH2Cl2) to afford the title compound as a off white gummy material (0.035 g, 29.%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09226500B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-e21419f4f48141cd97e585378fc8e864 |
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| Source note | uspto-grants-2016_01 |
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