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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040874Generated: November 1, 2026

6-Methyl-2-(4-methylene-1-piperidyl)-3-nitropyridine → 3-[(6-Methylpyridin-2-yl)ethynyl]-8-pyridin-2-yl-1-oxa-2-azaspiro[4.5]dec-2-ene-8-carbonitrile

https://huagongshe.com/reaction/2040874

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Methyl-2-(4-methylene-1-piperidyl)-3-nitropyridineHCID 57493810—
Reactant8-(2-Pyridyl)-2-(2-trimethylsilylethynyl)-4-oxa-3-azaspiro[4.5]dec-2-ene-8-carbonitrileHCID 57493846—
Product3-[(6-Methylpyridin-2-yl)ethynyl]-8-pyridin-2-yl-1-oxa-2-azaspiro[4.5]dec-2-ene-8-carbonitrileHCID 56643609—

Reaction Steps

The title compound was prepared following the method described for the compound of Example 3, replacing Compound 3c with Compound 48b. The crude was purified by automated flash chromatography (SP1®TM-Biotage; gradient Petroleum ether-EtOAc from 65:35 to 4:6) to give the title compound as yellow oil. Yield: 43.4%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580962B2
Source datasetuspto-grants-2013_11
ORD IDord-f1a935ea5dab4695a47b79b53d0c3c42
Source noteuspto-grants-2013_11