HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434295Generated: October 30, 2026
Triethylamine → (E)-N-{(R)-1-Benzyl-2-[4-(4-fluoro-benzoyl)-piperidin-1-yl]-ethyl}-3-(3-cyano-phenyl)-acrylamide
https://huagongshe.com/reaction/434295
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (2E)-3-(4-Cyanophenyl)-2-propenoic acid | HCID 735786 | — |
| Reactant | [1-((R)-2-amino-3-phenyl-propyl)-piperidin-4-yl]-(4-fluoro-phenyl)-methanone | HCID 68809327 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (E)-N-{(R)-1-Benzyl-2-[4-(4-fluoro-benzoyl)-piperidin-1-yl]-ethyl}-3-(3-cyano-phenyl)-acrylamide | HCID 68811168 | — |
Reaction Steps
To a solution of (E)-3-(4-cyano-phenyl)-acrylic acid (0.042 g, 0.242 mmol) in dichloromethane (1 ml) is added triethylamine (0.046 ml, 0.331 mmol) and (benzotriazo-1-yloxy)tripyrrolidino-phosphonium hexafluorophosphate (0.126 g, 0.242 mmol). The reaction mixture is stirred at ambient temperature for 5 minutes and then a solution of [1-((R)-2-amino-3-phenyl-propyl)-piperidin-4-yl]-(4-fluoro-phenyl)-methanone (0.075, 0.220 mmol) in dichloromethane (1 ml) is added. Stirring is continued for a further 3 hours, then the reaction mixture is diluted with dichloromethane (25 ml) and washed with saturated sodium bicarbonate solution and saturated brine. The dichloromethane is dried over magnesium sulphate and the solvent evaporated. The crude product is purified by flash silica chromatography (ethyl acetate:hexane, 5:1 elution) to afford (E)-N-{(R)-1-Benzyl-2-[4-(4-fluoro-benzoyl)-piperidin-1-yl]-ethyl}-3-(3-cyano-phenyl)-acrylamide. [MH]+496.8.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06670379B2 |
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| Source dataset | uspto-grants-2003_12 |
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| ORD ID | ord-de0dce3901a64251a9300f21e91b5f90 |
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| Source note | uspto-grants-2003_12 |
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