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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490199Generated: October 30, 2026

Formaldehyde → HCID 68872775, compound

https://huagongshe.com/reaction/490199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantPotassium CarbonateHCID 11430—
Reactant3-ChlorobenzamideHCID 69254—
Reactant1-(2-Pyridyl)piperazineHCID 94459—
SolventEthanolHCID 702—
ProductHCID 68872775HCID 6887277578.6%

Reaction Steps

A mixture of 1-pyridin-2-ylpiperazine (16 mg, 0.1 mmol, Aldrich), paraformaldehyde (30 mg, 1 mmol), 3-chlorobenzamide (78 mg, 0.5 mmol, Maybridge), and 42 mg of potassium carbonate (0.3 mmol) in 2 mL absolute ethyl alcohol was heated to reflux under nitrogen overnight. The mixture was cooled to room temperature, filtered, and the solvent was removed under reduced pressure. The residue was purified by flash column chromatography on silica gel (10% methanol:ethyl acetate) to give 26 mg (52%) pure compound; 1H NMR (500 MHz, DMSO-d6) δ 2.58 (t, J=4 Hz, 4H), 3.50 (t, J=4 Hz, 4H), 4.19 (d, J=5 Hz, 1H), 6.62 (t, J=5 Hz, 1H), 6.81 (d, J=6 Hz, 1H), 7.51 (m, 2H), 7.61 (m, 1H), 7.82 (d, J=6 Hz, 1H), 7.92 (s, 1H), 8.12 (d, J=5 Hz, 1H), 8.93 (t, J=5 Hz, 1H); MS (ESI/APCI−) m/e 329 (M−H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528134B2
Source datasetuspto-grants-2009_05
ORD IDord-879ed77d69c24bf28cec53825d1ae59a
Source noteuspto-grants-2009_05