Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896044Generated: October 31, 2026

2-Chloro-6-methyl-3-nitropyridine → 2-[1-(6-Methyl-3-nitropyridin-2-yl)piperidin-4-yl]but-3-yn-2-ol

https://huagongshe.com/reaction/1896044

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-6-methyl-3-nitropyridineHCID 1268230—
Reactant3-(6-Methyl-pyridin-2-yl)-1-piperidin-4-yl-prop-2-yn-1-olHCID 68977495—
Reactant2-(Piperidin-4-yl)but-3-yn-2-olHCID 86627358—
Product2-[1-(6-Methyl-3-nitropyridin-2-yl)piperidin-4-yl]but-3-yn-2-olHCID 8662735793%

Reaction Steps

The title compound was prepared as described for the compound of Example 237 but starting from Compound 312b instead of Compound 237a and 2-chloro-6-methyl-3-nitropyridine instead of 2-bromo-3-nitropyridine. After the work-up, the residue was purified by automated flash liquid chromatography (Horizon™-Biotage) eluting with PE-EtOAc from PE:EtOAc 9:1 affording the title products as yellow oil. Yield: 93%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518916B2
Source datasetuspto-grants-2013_08
ORD IDord-a12fff2d69c64735afc46742a3efac5a
Source noteuspto-grants-2013_08