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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850682Generated: October 30, 2026

(R)-4-chloro-6-((1-methylpiperidin-3-yl)oxy)pyrimidin-5-amine → (R)-4((1-methylpiperidin-3-yl)oxy)pyrimidin-5-amine

https://huagongshe.com/reaction/1850682

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-4-chloro-6-((1-methylpiperidin-3-yl)oxy)pyrimidin-5-amineHCID 90411331—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product(R)-4((1-methylpiperidin-3-yl)oxy)pyrimidin-5-amineHCID 9041165399%

Reaction Steps

(R)-4-chloro-6-((1-methylpiperidin-3-yl)oxy)pyrimidin-5-amine was dissolved in MeOH (15.0 mL) and Pd/C 10% (324.5 mg, 0.3049 mmol) was added and the reaction mixture stirred under a hydrogen atmosphere for 2 h. The reaction vessel was evacuated and flushed with nitrogen (3×), filtered through a celite pad washing with methanol followed by ethyl acetate. The combined filtrates were concentrated in vacuo to leave the title product 7a as a colourless oil (631 mg, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957078B2
Source datasetuspto-grants-2015_02
ORD IDord-5811122b801a46ee9ccb51820b1fdb65
Source noteuspto-grants-2015_02