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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216007Generated: October 29, 2026

Piperidine → HCID 86637703, compound

https://huagongshe.com/reaction/216007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 86637704HCID 86637704—
SolventEthanolHCID 702—
ProductHCID 86637703HCID 86637703131.3%

Reaction Steps

41-[3-[4-(p-chlorophenyl)-5-phenyl-(-[1,2,3]triazol-2-yl)]-3-bromopropane (26 mg, 0.07 mmol) and piperidine (9 mg, 0.10 mmol) were refluxed in ethanol for 1 h in presence of dry sodium carbonate (11 mg, 0.10 mmol). The reaction mixture was then filtrated. The solid was washed with CH2Cl2. The combined filtrates was evaporated in vacuo. The resulting oil was then purified by chromatography on silica gel eluting with EtOAc to afford 1-[3-[4-(p-chlorophenyl)-5-phenyl-(-[1,2,3]triazol-2-yl)propyl]-piperidine (35 mg, 75% yield); 1H NMR (200 MHz, CDCl3, 25° C.) δ=7.53-7.46 (4H, m), 7.39-7.31 (5H, m), 4.52 (2H, t, 3J=7.1 Hz), 2.46-2.39 (6H, m), 2.23 (2H, qt, 3J=7.2 Hz), 1.58 (4H, qt, 3J=5.5 Hz), 1.42 (2H, qt, 3J=5.5 Hz) ppm. ES-MS: m/z=382 (5), 381 (4), 380 (14) [M+●]; 98 (100) [M-283]; 84 (30) [M-297].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193223B2
Source datasetuspto-grants-2012_06
ORD IDord-818d882720a140e8a483065250d1459f
Source noteuspto-grants-2012_06