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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1876827Generated: November 2, 2026

1-(2-Methoxyphenyl)piperazine → HCID 66881744, compound

https://huagongshe.com/reaction/1876827

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Methoxyphenyl)piperazineHCID 1346—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 66882500HCID 66882500—
SolventAcetoneHCID 180—
ProductHCID 66881744HCID 6688174493%

Reaction Steps

To a stirred suspension of [4-(3-bromopropyloxy)-5-methoxy-2-nitrophenyl][4-(2-methoxyphenyl)piperazino]methanone (9) (500 mg, 1.65 mmol), 1-(2-methoxyphenyl)piperazine (316 mg 15.6 mmol) and K2CO3 (816 mg 26.6 mmol) in acetone (30 mL) and the stirring was continued for 16 h. The acetone was evaporated in vacuum and the aqueous layer was washed with ethyl acetate and extracted with ethyl acetate and washed with brine, dried over Na2SO4 and evaporated in vacuum to afford the crude product to (5-methoxy-4-3-[4-(2-methoxyphenyl)-piperazino]propoxy-2-nitrophenyl)[4-(2-methoxyphenyl)piperazino]methanone (10) in 93% yield (670 mg, 85% yield). 1H NMR (CDCl3): δ 1.60-2.15 (m, 2H), 2.98-3.12 (t, 2H, J=7.31 Hz), 3.18-3.36 (m, 8H), 3.38-3.60 (m, 10H), 3.85 (m, 3H), 3.95 (s, 3H), 4.00-4.15 (m, 3H) 6.85-7.00 (m, 8H), 7.20-7.40 (m, 1H), 7.70-7.80 (d, 1H, J=6.81 Hz); FABMS: 619 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309726B2
Source datasetuspto-grants-2012_11
ORD IDord-9670291fc0e84b1ab8ba58db096f840d
Source noteuspto-grants-2012_11