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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49838Generated: October 27, 2026

Pyridine → HCID 12096564, compound

https://huagongshe.com/reaction/49838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactantp-Anisoyl chlorideHCID 7477—
ReactantN1-[1-(4-pyridyl)piperidin-4-ylmethyl)-1,2-benzenediamineHCID 12150698—
SolventChloroformHCID 6212—
ProductHCID 12096564HCID 1209656417%

Reaction Steps

A solution of N1-[1-(4-pyridyl)piperidin-4-ylmethyl]-1,2-benzenediamine (212 mg, 0.75 mmol) and pyridine (4 mL) in chloroform (2 mL) at 0° C. was treated with a solution of 4-methoxybenzoyl chloride (128 mg, 0.75 mmol) in chloroform. The mixture was allowed to warm to room temperature and stir for 17 h. The mixture was concentrated and the residue was dissolved in EtOAc. The organic layer was washed with 1 N NaOH (2×), water (3×), brine (1×), dried (K2CO3), and concentrated. The residue was purified by RPHPLC, yielding 52 mg (17%) of the title compound as a hydrochloride salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710057B2
Source datasetuspto-grants-2004_03
ORD IDord-31d897344a7b4712a42d649466f39479
Source noteuspto-grants-2004_03