HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610774Generated: October 31, 2026
Benzylethanolamine → N-cyclohepty-5-[benzyl(2-hydroxyethyl)amino]pentanamide
https://huagongshe.com/reaction/610774
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzylethanolamine | HCID 4348 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | n-Cycloheptyl-5-bromopentanamide | HCID 22125969 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-cyclohepty-5-[benzyl(2-hydroxyethyl)amino]pentanamide | HCID 22125972 | 58.5% |
Reaction Steps
N-cycloheptyl-5-bromopentanamide (4.15 g, 15 mmole) in solution in dimethylformamide (20 ml) is added dropwise to a hot solution (60° C.) of N-benzylethanolamine (2.27 g, 2.13 ml, 15 mmole) in dimethylformamide (25 ml) in the presence of potassium carbonate (4.15 g, 3 mmole). The reaction mixture is agitated for 2 hours at 60° C. then the solvent is evaporated under reduced pressure. The residue is taken up in dichloromethane (50 ml) and washed with water (3×30 ml). The organic phase is collected, dried over magnesium sulfate; the solvent is evaporated under reduced pressure. The product obtained is purified by flash chromatography over silica gel in a mixture of dichloromethane/methanol (90/10) to give 3.04 g (50%) of the expected compound in the form of an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05998666 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-fadcc4f3ec5f43bab5e96e01299add98 |
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| Source note | uspto-grants-1999_12 |
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