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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193381Generated: November 1, 2026

Benzyl 1-(6-(dimethylamino)pyridin-3-yl)piperidin-4-yl(methyl)carbamate → N,N-Dimethyl-5-(4-(methylamino)piperidin-1-yl)pyridin-2-amine

https://huagongshe.com/reaction/1193381

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 1-(6-(dimethylamino)pyridin-3-yl)piperidin-4-yl(methyl)carbamateHCID 66799303—
SolventMethanolHCID 887—
ProductN,N-Dimethyl-5-(4-(methylamino)piperidin-1-yl)pyridin-2-amineHCID 6679860394%

Reaction Steps

Benzyl 1-(6-(dimethylamino)pyridin-3-yl)piperidin-4-yl(methyl)carbamate (400 mg, 1.086 mmol, 1.0 eq.) was dissolved in MeOH (10 ml) and degassed with argon. Pd(OH)2 (200 mg) was then added and hydrogenation was carried out for 3 hours. After monitoring by TLC, the reaction mixture was filtered over Celite, the filtrate was concentrated under reduced pressure and the crude product was used in the next stage without being purified further. Yield: 94% (240 mg, 1.0212 mmol)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680159B2
Source datasetuspto-grants-2014_03
ORD IDord-f4a2f56079bf407dbde3ceb13714c4ac
Source noteuspto-grants-2014_03