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HRID 1937322Erstellt: 26. Oktober 2026

1-(6-Bromonaphthalene-2-sulfonyl)piperazine → HCID 178452975, Verbindung

https://huagongshe.com/reaction/1937322

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(6-Bromonaphthalene-2-sulfonyl)piperazineHCID 22329709—
EduktHCID 178452976HCID 178452976—
LösungsmittelEthanolHCID 702—
ProduktHCID 178452975HCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06395731B1
Quelldatensatzuspto-grants-2002_05
ORD IDord-e78264ba1e06400485a35fa465dbefa3
Quellennotizuspto-grants-2002_05