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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415722Generated: November 1, 2026

Acetone → HCID 22636122, compound

https://huagongshe.com/reaction/2415722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantPotassium CarbonateHCID 11430—
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 22636163HCID 22636163—
SolventEthyl AcetateHCID 8857—
ProductHCID 22636122HCID 2263612241.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

N-Methylpiperazine (0.036 g) was added to a mixture of 3-(3-chloromethylbenzamido)-4-methyl-N-(3-morpholinophenyl)benzamide (0.15 g), potassium carbonate (0.09 g) and acetone (5 ml) and the resultant mixture was stirred and heated to 60° C. for 16 hours. The mixture was evaporated and the residue was partitioned between methylene chloride and a saturated aqueous sodium bicarbonate solution. The organic phase was dried over magnesium sulphate and evaporated. The residue was purified by column chromatography on silica gel using methanol as eluent. The product so obtained was dissolved in ethyl acetate and precipitated by the addition of isohexane. There was thus obtained the title compound (0.071 g); NMR Spectrum: (DMSOd6) 2.1 (s, 3H), 2.3 (s, 3H), 2.2-2.4 (m, 8H), 3.1 (t, 4H), 3.55 (s, 2H), 3.75 (t, 4H), 6.65-6.7 (m, 1H), 7.18 (t, 1H), 7.3-7.35 (m, 1H), 7.38-7.55 (m, 4H), 7.78-7.8 (m, 1H), 7.85-7.9 (m, 2H), 7.95 (s, 1H); Mass Spectrum: M+H+ 528.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06821965B1
Source datasetuspto-grants-2004_11
ORD IDord-2ca8789ab80949c0a5fed5519f1aeca2
Source noteuspto-grants-2004_11