HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(1-benzylpiperidin-4-yl)-4-amino-2,3,5,6-tetrachloropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Benzyl-4-piperidylamine | HCID 415852 | — |
| Reactant | 2,3,5,6-Tetrachloro-4-nitropyridine | HCID 15229167 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-(1-benzylpiperidin-4-yl)-4-amino-2,3,5,6-tetrachloropyridine | HCID 19068076 | 89.4% |
Reaction Steps
8.7 g 1-benzyl-4-aminopiperidine, 4.6 g triethylamine and 10 g 4-nitro-2,3,5,6-tetrachloropyridine was added to 100 ml absolute dioxane and stirred for 5 hours at room temperature. After removing dioxane by distillation, the residue was taken up in methylene chloride, admixed with 2 normal hydrochloric acid and stirred vigorously for 30 min. The precipitated precipitate was separated, taken up in a small amount of water, made alkaline with 2 normal ammonia and the aqueous solution was extracted several times with dichloromethane. 13.9 g N-(1-benzylpiperidin-4-yl)-4-amino-2,3,5,6-tetrachloropyridine is obtained as an oil. TLC (mobile solvent: toluene/dioxane/water 9:4.5:0.5), Rf=0.6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05786371 |
| Source dataset | uspto-grants-1998_07 |
| ORD ID | ord-2fc2d71eab3f462c8d1b1b873e091c61 |
| Source note | uspto-grants-1998_07 |