HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2373644Erstellt: 24. Oktober 2026
Diisopropylethylamine → N-(3-{2-[4-(2-methyl-5-quinazolinyl)-1-piperazinyl]ethyl}phenyl)methanesulfonamide
https://huagongshe.com/de/reaction/2373644
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | HCID 57444358 | HCID 57444358 | — |
| Edukt | 2-{3-[(Methylsulfonyl)amino]phenyl}ethyl methanesulfonate | HCID 57444359 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | N-(3-{2-[4-(2-methyl-5-quinazolinyl)-1-piperazinyl]ethyl}phenyl)methanesulfonamide | HCID 57444357 | 37,6% |
Reaktionsschritte
A mixture of 2-methyl-5-(1-piperazinyl)quinazoline (50 mg), 2-{3-[(methylsulfonyl)amino]phenyl}ethyl methanesulfonate (65 mg), diisopropylethylamine (192 μL) and DMF (0.5 mL) was heated to 100° C. in a sealed tube and stirred for 24 hours. The mixture was cooled to room temperature and partitioned between aqueous ammonium chloride solution and ethyl acetate. The organic layer was washed (water, brine), dried (sodium sulfate) and concentrated in vacuo. The residue was purified by column chromatography [SiO2; DCM-MeOH: (100:0)→(95:5)] to give the title compound as a beige foam (35 mg).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07459456B2 |
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| Quelldatensatz | uspto-grants-2008_12 |
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| ORD ID | ord-244d5e038dd94076baad4e85bf3aa668 |
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| Quellennotiz | uspto-grants-2008_12 |
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