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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15843Generated: October 25, 2026

1-(3-Bromophenyl)propan-2-one → 5-{4-[2-(3-Bromophenyl)propyl]-1-piperazinyl)-2-methylquinoline

https://huagongshe.com/reaction/15843

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Bromophenyl)propan-2-oneHCID 2734093—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant3-(2-[4-(2-Methyl-5-quinolinyl)-1-piperazinyl]ethyl}anilineHCID 49852105—
CatalystZincchlorideHCID 3007855—
SolventMethanolHCID 887—
Product5-{4-[2-(3-Bromophenyl)propyl]-1-piperazinyl)-2-methylquinolineHCID 5744432850%

Reaction Steps

A solution of zinc(II) chloride (0.5 M, THF, 0.5 eq., 234 uL) was added to a stirred solution of 1-(3-bromophenyl)-2-propanone (50 mg) and 2-methyl-5-(1-piperazinyl)quinoline (D3) (2.0 eq., 107 mg) in methanol (1 ml). The mixture was stirred 10 minutes then a solution of sodium cyanoborohydride (1M, THF, 1.0 eq., 234 uL) was added. The resulting white mixture was stirred at room temperature until hplc showed the complete disappearance of starting material. The mixture was concentrated under reduced pressure, diluted with aqueous sodium hydroxide solution (1M), and extracted with DCM. The combined organic phases were washed with brine, dried over sodium sulfate and concentrated. The crude was purified by chromatography using a SPE cartridge (SiO2) with DCM-methanol (98:2) as eluent to afford the title compound (50 mg, 50% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732600B2
Source datasetuspto-grants-2010_06
ORD IDord-0e4db506b4a34fef99d9172f3bc427fc
Source noteuspto-grants-2010_06