HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610775Generated: October 26, 2026
Triethylamine → N-cycloheptyl-5-[benzyl(2-chloroethyl)amino]pentanamide
https://huagongshe.com/reaction/610775
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | N-cyclohepty-5-[benzyl(2-hydroxyethyl)amino]pentanamide | HCID 22125972 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-cycloheptyl-5-[benzyl(2-chloroethyl)amino]pentanamide | HCID 22125964 | 100.5% |
Reaction Steps
Methanesulfonyl chloride (0.78 g, 0.52 ml, 6.6 mmole) is added dropwise with stirring to a cooled solution of N-cycloheptyl-5-[benzyl(2-hydroxyethyl)amino]pentanamide (2.14 g, 6 mmole) in dichloromethane (20 ml) in the presence of triethylamine (0.69 g, 0.94 ml, 6.6 mmole). Agitation is maintained for 18 hours at 20° C. The reaction mixture is filtered with iced water (25 ml) then dried over magnesium sulfate. Filtration and evaporation of the solvent under reduced pressure give 2.2 g (98%) of the desired 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-ad769e8ded184b9ca87d1d74bdef8ed9 |
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| Source note | uspto-grants-1999_12 |
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