HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503677Generated: October 31, 2026
Diisopropylethylamine → HCID 86675140, compound
https://huagongshe.com/reaction/1503677
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 DCM (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 RT. The reaction mixture was stirred at RT for 5 h. The reaction mixture was diluted with DCM. The combined DCM layer was washed with 3N HCl and saturated NaHCO3 solution, the separated DCM 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% methanol in DCM) to afford the title compound as an off white gummy material (0.035 g, 29.%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09212164B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-a970452887b84af2a870c0019cb58d38 |
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| Source note | uspto-grants-2015_12 |
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