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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048335Generated: November 1, 2026

2-Chloro-3-methyl-5-nitropyridine → (3S,5R,6S)-3-allyl-5-(3-chlorophenyl)-6-(4-chlorophenyl)-3-methyl-1-(3-methyl-5-nitropyridin-2-yl)piperidin-2-one

https://huagongshe.com/reaction/1048335

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-3-methyl-5-nitropyridineHCID 89648—
Reactant(3S,5R,6S)-3-allyl-5-(3-chlorophenyl)-6-(4-chlorophenyl)-3-methylpiperidin-2-oneHCID 58574008—
Product(3S,5R,6S)-3-allyl-5-(3-chlorophenyl)-6-(4-chlorophenyl)-3-methyl-1-(3-methyl-5-nitropyridin-2-yl)piperidin-2-oneHCID 67998434—

Reaction Steps

The title compound was prepared from (3S,5R,6S)-3-allyl-5-(3-chlorophenyl)-6-(4-chlorophenyl)-3-methylpiperidin-2-one (Example 71, Step D) and 2-chloro-3-methyl-5-nitropyridine as described in Example 111, Step A to provide a light-yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569341B2
Source datasetuspto-grants-2013_10
ORD IDord-cf1dd1eabfba4112b782296cdf2e4615
Source noteuspto-grants-2013_10