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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(3-Bromophenyl)propan-2-one | HCID 2734093 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 3-(2-[4-(2-Methyl-5-quinolinyl)-1-piperazinyl]ethyl}aniline | HCID 49852105 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-{4-[2-(3-Bromophenyl)propyl]-1-piperazinyl)-2-methylquinoline | HCID 57444328 | 50% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07732600B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-0e4db506b4a34fef99d9172f3bc427fc |
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| Source note | uspto-grants-2010_06 |
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