HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 271140Erstellt: 26. Oktober 2026
Diisopropylethylamine → 3-Phenylsulfonyl-8-piperazin-1-yl-quinoline hydrochloride
https://huagongshe.com/reaction/271140
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Edukt | 8-(4-Methyl-piperazin-1-yl)-3phenylsulfonylquinoline | HCID 9929162 | — |
| Lösungsmittel | 1,2-Dichloroethane | HCID 11 | — |
| Produkt | 3-Phenylsulfonyl-8-piperazin-1-yl-quinoline hydrochloride | HCID 56972141 | 52,5% |
Reaktionsschritte
A stirred solution of 8-(4-methyl-piperazin-1-yl)-3-phenylsulfonylquinoline (E1) (0.148 g, 0.4 mmol), 1-chloroethyl chloroformate (0.093 ml, 0.85 mmol) and N,N-diisopropylethylamine (0.148 ml, 0.85 mmol) in 1,2-dichloroethane (9 ml) was heated at reflux for 1.25 h under argon. The reaction mixture was cooled to ambient temperature and concentrated in vacuo to an oil. The oil was purified by chromatography over silica gel eluting with a gradient of methanol/dichloromethane, pooling fractions which contained the major component (Rf 0.9, methanol/dichloromethane 1:19). The purified material was redissolved in methanol (15 ml) and the solution was refluxed for 1 h under argon. The reaction mixture was cooled to ambient temperature and concentrated in vacuo to a solid which was stirred with diethyl ether (5 ml) and filtered to afford the title compound (E2) (0.08 g, 0.21 mmol, 51%);
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07452888B2 |
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| Quelldatensatz | uspto-grants-2008_11 |
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| ORD ID | ord-84a66ae5de5f446a84b156f158c410f9 |
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| Quellennotiz | uspto-grants-2008_11 |
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