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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774312Generated: November 3, 2026

Potassium Carbonate → HCID 86713095, compound

https://huagongshe.com/reaction/1774312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantBromomethyl 3-methoxyphenyl ketoneHCID 101294—
ReactantHCID 71061917HCID 71061917—
SolventAcetonitrileHCID 6342—
ProductHCID 86713095HCID 86713095—

Reaction Steps

A stirred mixture of 2-bromo-1-(3-methoxyphenyl)ethanone (0.5 g, 2.2 mmol), 1-[3-(2-pyridyl)-2-pyridyl]piperazine (0.6 g, 2.6 mmol) and K2CO3 (3 mmol) in acetonitrile was refluxed overnight. After cooling, the mixture was evaporated to dryness and H2O (20 mL) was added to the residue. The aqueous phase was extracted with AcOEt (2×30 mL). The collected organic layers were dried over Na2SO4 and evaporated under reduced pressure. The crude residue was chromatographed (CHCl3/AcOEt, 9:1, as eluent) to afford pure compound in quantitative yield. 1H NMR (CDCl3): δ 2.52 (br s, 4H), 2.93 (app t, 4H), 3.78 (s, 2H), 3.80 (s, 3H), 6.84-6.90 (m, 3H), 7.04-7.10 (m, 2H) 7.20-7.26 (m, 1H), 7.71 (dd, 1H, J=1.6, 7.4 Hz), 7.83 (dt, 1H, J=1.9, 7.4 Hz), 7.88-7.92 (m, 1H), 8.27 (dd, 1H, J=1.9, 4.9 Hz), 8.69-8.72 (m, 1H). GC-MS m/z 387 (M+1, 2), 390 (M+, 8), 254 (100), 184 (63).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260400B2
Source datasetuspto-grants-2016_02
ORD IDord-a56bbae43ca44ebb880de4f23d0a35cd
Source noteuspto-grants-2016_02