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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373614Generated: October 31, 2026

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

https://huagongshe.com/reaction/2373614

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—
SolventMethanolHCID 887—
Product5-{4-[2-(3-Bromophenyl)propyl]-1-piperazinyl)-2-methylquinolineHCID 5744432850%

Reaction Steps

A solution of zinc(ll)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 numberUS07459456B2
Source datasetuspto-grants-2008_12
ORD IDord-13c2cac0317042c2be08b2d716d0cb86
Source noteuspto-grants-2008_12