HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 5,6-Dichloro-N-ethylnicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethylamine hydrochloride | HCID 11198 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5,6-Dichloro-N-ethylnicotinamide | HCID 20120133 | 85% |
Reaction Steps
A round bottomed flask was charged with 5,6-dichlorornicotic acid (30 g, 156 mmol), ethylamine HCl salt (14 g, 170 mmol), dimethylformamide (300 ml), dichloromethane (100 ml), triethylamine (26.1 ml, 187 mmol), and 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (32.9 g, 170 mmol). The reaction mixture was stirred at room temperature overnight. The solvent was removed in vacuo, the residue was dissolved in ethyl acetate (500 mL) and was washed with 1N HCl (2×), saturated aqueous sodium bicarbonate (1×), brine (1×), and dried over magnesium sulfate. The solution was filtered and concentrated in vacuo to provide the desired 5,6-Dichloro-N-ethyl-nicotinamide 2 (29 g, 85%). MS: M+H=219.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07776862B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-d6eecdb230794df0985b83146d26e8ca |
| Source note | uspto-grants-2010_08 |