HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1937322Erstellt: 26. Oktober 2026
1-(6-Bromonaphthalene-2-sulfonyl)piperazine → HCID 178452975, Verbindung
https://huagongshe.com/reaction/1937322
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-(6-Bromonaphthalene-2-sulfonyl)piperazine | HCID 22329709 | — |
| Edukt | HCID 178452976 | HCID 178452976 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | HCID 178452975 | HCID 178452975 | — |
Reaktionsschritte
The requisite 1-(6-bromonaphth-2-ylsulphonyl)-4-[4-(2-t-butyloxycarbonylaminoimidazol-4-yl)benzoyl]piperazine starting material was prepared by a coupling method exactly analogous to that described in Example 1, starting from 4(2-t-butyloxycarbonylaminoimidazol-4-yl)benzoic acid and 1-(6-bromonaphth-2-ylsulphonyl)piperazine, to give 1-(6-bromonaphth-2-ylsulphonyl)-4-[4-(2-t-butyloxycarbonylaminoimidazol-4-yl)benzoyl]piperazine as a colourless solid (after trituration with hot ethanol) (248 mg, 40% yield), m.p. 175-177° C., 1H NMR (d6DMSO) 1.5 ppm (s,9H), 3.0-3.1 ppm (broad s,4H), 3.4-3.7 ppm (broad s,4H), 6.6 ppm (s,2H), 7.3 ppm (d,2H), 7.4 ppm (s,1H), 7.7 ppm (d,2H), 7.8 ppm (t,2H), 8.2 ppm (t,2H), 8.4 ppm (s,1H), 8.45 ppm (s,1H); MS (M+H)+ 640/642 (w), (M+H-56)+ 584/585 (s), loss of C4H8.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06395731B1 |
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| Quelldatensatz | uspto-grants-2002_05 |
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| ORD ID | ord-e78264ba1e06400485a35fa465dbefa3 |
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| Quellennotiz | uspto-grants-2002_05 |
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