HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15894Generated: October 31, 2026
Diisopropylethylamine → 5-{4-[2-(3-Iodophenyl)ethyl]-1-piperazinyl)2-methylquinoline
https://huagongshe.com/reaction/15894
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-(2-[4-(2-Methyl-5-quinolinyl)-1-piperazinyl]ethyl}aniline | HCID 49852105 | — |
| Reactant | 2-(3-Iodophenyl)ethyl methanesulfonate | HCID 57444370 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-{4-[2-(3-Iodophenyl)ethyl]-1-piperazinyl)2-methylquinoline | HCID 57444355 | 86.7% |
Reaction Steps
N,N-Diisopropylethylamine (1.7 mL; 1.5 eq) was added to a solution of 2-methyl-5-(1-piperazinyl)quinoline (D3) (1.31 g; 0.9 eq) and 2-(3-iodophenyl)ethyl methanesulfonate (2.1 g) in dimethylformamide (20 mL). The reaction mixture was heated to 90° C. for 5 hours. The dark solution was concentrated under reduced pressure, and purified by ion-exchange chromatography (SCX-2), eluting with methanol-ammonia/methanol (1M), (1:0) to (0:1). The combined basic fractions were concentrated under vacuum and purified by column chromatography (SPE cartridge, SiO2) using dichloromethane-methanol (95:5) to afford the title compound (1.5 g, 60% 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-74b35ab596ad4432bd7a38ffa65b7cee |
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| Source note | uspto-grants-2010_06 |
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