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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916938Generated: November 1, 2026

1-Aminopiperidine → HCID 44390753, compound

https://huagongshe.com/reaction/916938

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-AminopiperidineHCID 16658—
ReactantHCID 86600271HCID 86600271—
SolventDichloromethaneHCID 6344—
ProductHCID 44390753HCID 44390753—

Reaction Steps

To a portion of the methylene chloride (1 mL) solution of 2-(chloro)-6-(2,4-dichlorophenyl)-5-(4-chlorophenyl)pyridine-3-carbonyl chloride (0.068 mmol) from Step B was added a solution of 1-aminopiperidine (0.010 mL, 0.088 mmol) and TEA (0.014 mL, 0.10 mmol) in methylene chloride (1 mL). The reaction was stirred at rt for 16 h and was then evaporated. The residue was purified by preparative TLC (40% ethyl acetate in hexanes) to yield N-(piperidin-1-yl)-2-(chloro)-6-(2,4-dichlorophenyl)-5-(4-chlorophenyl)pyridine-3-carboxamide. HPLC/MS: 494 (M+1), 496 (M+3); Rt=3.97 min

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07271266B2
Source datasetuspto-grants-2007_09
ORD IDord-8ef73c9ef99c479d981b2a50e240fba5
Source noteuspto-grants-2007_09