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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1977605Generated: October 25, 2026

4-(Chloromethyl)pyridinium chloride → 3-[3-(2-indanyloxy)-4-methoxy-N-(4-pyridylmethyl)anilino]-2-methyl-2-cyclopenten-1-one

https://huagongshe.com/reaction/1977605

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Chloromethyl)pyridinium chlorideHCID 74570—
Reactant3-[3-(2-Indanyloxy)-4-methoxyanilino]-2-methyl-2-cyclopenten-1-oneHCID 9863185—
Product3-[3-(2-indanyloxy)-4-methoxy-N-(4-pyridylmethyl)anilino]-2-methyl-2-cyclopenten-1-oneHCID 2199445038.8%

Reaction Steps

According to the same procedure as in Example 28, using 3-[3-(2-indanyloxy)-4-methoxyanilino]-2-methyl-2-cyclopenten-1-one produced in Example 10 instead of 3-(3-cyclopentyloxy-4-methoxyanilino)-2-cyclopenten-1-one, and using 4-(chloromethyl)pyridine hydrochloride instead of methyl iodide, the title compound (yield 38.8%) was obtained as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06235736B1
Source datasetuspto-grants-2001_05
ORD IDord-64ee173c34894fd386fa3d87085d74ed
Source noteuspto-grants-2001_05