HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494626Generated: October 27, 2026
Triethylamine → 3-((methylamino)carbonyl)-N-(2,4,6-trichlorophenyl)-1-piperazineacetamide
https://huagongshe.com/reaction/1494626
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-chloro-N-(2,4,6-trichlorophenyl)acetamide | HCID 31122 | — |
| Reactant | N-Methylpiperazine-2-carboxamide | HCID 14722545 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | 3-((methylamino)carbonyl)-N-(2,4,6-trichlorophenyl)-1-piperazineacetamide | HCID 14722546 | 24.4% |
Reaction Steps
A mixture of 15.33 parts of N-methyl-2-piperazinecarboxamide, 27.2 parts of 2-chloro-N-(2,4,6-trichlorophenyl)acetamide, 9.8 parts of N,N-diethylethanamine and 300 parts of 2-methoxyethanol was stirred for 3 hours at 60° C. The reaction mixture was evaporated. The residue was taken up in a small amount of water and treated with sodium carbonate. The product was extracted three times with dichloromethane. The combined extracts were dried, filtered and evaporated. The residue was crystallized from acetonitrile. The product was filtered off (the filtrate was set aside) and dried, yielding a first fraction of 9.27 parts (24.4%) of 3-[(methylamino)carbonyl]-N-(2,4,6-trichlorophenyl)-1-piperazineacetamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05026853 |
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| Source dataset | uspto-grants-1991_06 |
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| ORD ID | ord-21271dff411842f99eece3dde9610f19 |
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| Source note | uspto-grants-1991_06 |
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