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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 346779Erstellt: 24. Oktober 2026

2-Methoxyaniline → N-(2-methoxyphenyl)4-(4-methyl-1-piperazinyl)-3-nitrobenzenesulfonamide

https://huagongshe.com/de/reaction/346779

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-MethoxyanilineHCID 7000—
EduktBenzenesulfonyl chloride, 4-chloro-3-nitro-HCID 7323—
Edukt1-MethylpiperazineHCID 53167—
Edukt4-chloro-N-(2-methoxyphenyl)-3-nitrobenzenesulfonamideHCID 2887683—
LösungsmittelPyridineHCID 1049—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(2-methoxyphenyl)4-(4-methyl-1-piperazinyl)-3-nitrobenzenesulfonamideHCID 22272549—

Reaktionsschritte

The compound was prepared from 4-chloro-3-nitrobenzenesulfonylchloride (1 g, 3.9 mmol), 2-methoxyaniline (0.53 mL, 4.7 mmol) and pyridine (1.6 mL) in CH2Cl2 (2 mL). 4-Chloro-N-(2-methoxyphenyl)-3nitrobenzenesulfonamide (0.345 mg) was reacted with N-methylpiperazine (0.144 mL) to afford N-(2-methoxyphenyl)-4-(4-methyl-1-piperazinyl)-3-nitrobenzenesulfonamide which was treated with Raney-Ni and hydrazine monohydrate. The final product was isolated as its HCl salt 1H NMR (DMSO-d6) δ 7.185 (dd, 1H), 7.08 (dt, 1H), 6.975 (d, 1H), 6.91–6.94 (m, 2H); 6.84 (dt, 1H), 3.56 (s, 3H), 3.42–3.47 (m, 2H), 3.22–3.24 (m, 2H), 2.95 (bt, 2H), 2.79 (bs, 3H); MS (posESI) m/z=376.2 (M+H+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07173035B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-1c163b124b904ec9a322f30962930c1d
Quellennotizuspto-grants-2007_02