HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81678Generated: October 27, 2026
1,2-Ethanediamine, N1,N1,N2-trimethyl- → 3-Chloro-N-[2-(dimethylamino)ethyl]-2-fluoro-N-methylisonicotinamide
https://huagongshe.com/reaction/81678
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Ethanediamine, N1,N1,N2-trimethyl- | HCID 67338 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | 3-Chloro-2-fluoropyridine-4-carboxylic acid | HCID 12175428 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-Chloro-N-[2-(dimethylamino)ethyl]-2-fluoro-N-methylisonicotinamide | HCID 68429843 | 85.8% |
Reaction Steps
N,N,N′-trimethylethane-1,2-diamine (0.92 ml, 6.84 mmol), 1-hydroxybenzotriazole monohydrate (1.05 g, 6.84 mmol) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (1.31 g, 6.84 mmol) were added to a chloroform solution (15 ml) of 3-chloro-2-fluoroisonicotinic acid (1.0 g, 5.70 mmol), and stirred under a nitrogen atmosphere at room temperature for 30 minutes. Saturated saline water was added to the reaction solution, and extracted with chloroform/methanol (9:1). The organic layer was dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by amine-type silica gel column chromatography (Biotage NH, hexane:ethyl acetate=4:1 to 1:1) to obtain 3-chloro-N-[2-(dimethylamino)ethyl]-2-fluoro-N-methylisonicotinamide (1.27 g, yield: 85%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08846700B2 |
|---|
| Source dataset | uspto-grants-2014_09 |
|---|
| ORD ID | ord-3312719c09ba4852a4dbc0e50dbc5fff |
|---|
| Source note | uspto-grants-2014_09 |
|---|