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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69917Generated: October 25, 2026

(S)-4-(3-(tert-butyldimethylsilyloxy)piperidin-1-yl)-3-nitropyridine → tert-butyl(S)-4-(3-(tert-butyldimethylsilyloxy)piperidin-1-yl)pyridin-3-amine

https://huagongshe.com/reaction/69917

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-4-(3-(tert-butyldimethylsilyloxy)piperidin-1-yl)-3-nitropyridineHCID 69095957—
SolventEthanolHCID 702—
Producttert-butyl(S)-4-(3-(tert-butyldimethylsilyloxy)piperidin-1-yl)pyridin-3-amineHCID 8666919167%

Reaction Steps

Following Method 2 of Example 49, (S)-4-(3-(tert-butyl dimethylsilyloxy)piperidin-1-yl)-3-nitropyridine in ethanol was reduced yielding tert-butyl (S)-4-(3-(tert-butyldimethylsilyloxy)piperidin-1-yl)pyridin-3-amine (67% yield 3 steps). LCMS (m/z): 308.2 (MH+); LC Rt=3.47 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822497B2
Source datasetuspto-grants-2014_09
ORD IDord-9d19944cd6754ea090aceaabf9c44164
Source noteuspto-grants-2014_09