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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957520Generated: November 2, 2026

Triethylamine → N-(1-benzylpiperidin-4-yl)-4-amino-2,3,5,6-tetrachloropyridine

https://huagongshe.com/reaction/1957520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Benzyl-4-piperidylamineHCID 415852—
Reactant2,3,5,6-Tetrachloro-4-nitropyridineHCID 15229167—
Solvent1,4-DioxaneHCID 31275—
ProductN-(1-benzylpiperidin-4-yl)-4-amino-2,3,5,6-tetrachloropyridineHCID 1906807689.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05786371
Source datasetuspto-grants-1998_07
ORD IDord-2fc2d71eab3f462c8d1b1b873e091c61
Source noteuspto-grants-1998_07