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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216773Generated: October 30, 2026

HCID 57707840, compound → HCID 57708002, compound

https://huagongshe.com/reaction/216773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57707840HCID 57707840—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 57708002HCID 57708002—

Reaction Steps

3-(Azidomethyl)-8-chloro-2-(piperidin-1-yl)quinoline (30 mg, 0.1 mmol) was dissolved in MeOH (1 mL) and treated with 10% Pd—C (5 wt %) and the mixture was then stirred under H2 balloon over night. The mixture was filtered through a Celite™ pad followed by removal of solvents to give (8-chloro-2-(piperidin-1-yl)-quinolin-3-yl)methanamine as a colorless oil. N-((8-chloro-2-(piperidin-1-yl)-quinolin-3-yl)methyl)-9H-purin-6-amine was prepared according to Procedure H. 1H NMR (400 MHz, CDCl3) δ ppm 8.29 (s, 1H), 7.79 (m, 3H), 7.45 (m, 2H), 5.43 (2H, s), 3.90 (m, 4H), 2.23 (m, 4H), 1.84 (m, 2H). Mass Spectrum (ESI) m/e=394 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193199B2
Source datasetuspto-grants-2012_06
ORD IDord-f7ef79a8e0184ed294d58ff32f7c31af
Source noteuspto-grants-2012_06