HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56079Generated: October 26, 2026
N,N'-Dimethylethylenediamine → HCID 72950843, compound
https://huagongshe.com/reaction/56079
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N'-Dimethylethylenediamine | HCID 8070 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 3,5-Dimethyl-1,2-dihydropyridin-2-one | HCID 12348538 | — |
| Reactant | N-ethyl-N-(2-fluoro-4-iodobenzyl)ethanamine | HCID 90022808 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 72950843 | HCID 72950843 | 14% |
Reaction Steps
To a solution of N-ethyl-N-(2-fluoro-4-iodobenzyl)ethanamine (1.72 g, 5.60 mmol) in dioxane (50 mL) was added 3,5-dimethyl-pyridone (0.69 g, 5.60 mmol), N,N′-dimethyl ethane-1,2-diamine (0.20 g, 2.24 mmol), CuI (0.21 g, 1.12 mmol) and potassium phosphate (2.38 g, 11.20 mmol) under N2. The reaction mixture was heated at 110° C. for 9 h, then cooled to rt and poured into CH2Cl2 (200 mL). The mixture was filtered, and the filtrate was washed with water (200 mL×3) and brine (200 mL). The organic phase was concentrated in vacuo. The residue was purified by a silica gel column chromatography (CH2Cl2/MeOH (V/V)=10:1) to give the title compound as a yellow solid (0.23 g, 14%). The compound was characterized by the following spectroscopic data:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434695B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-d8c55eb0ee28480caf5c4cd07449b078 |
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| Source note | uspto-grants-2016_09 |
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