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HRID 746741Erstellt: 24. Oktober 2026

N-Acetylsulfanilyl chloride → Methyl 2-{[2-({[4-(acetylamino)phenyl]sulfonyl}amino)phenyl]thio}benzoate

https://huagongshe.com/de/reaction/746741

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-Acetylsulfanilyl chlorideHCID 8481—
EduktMethyl 2-[(2-aminophenyl)sulfanyl]benzoateHCID 614949—
LösungsmittelPyridineHCID 1049—
LösungsmittelEthyl AcetateHCID 8857—
ProduktMethyl 2-{[2-({[4-(acetylamino)phenyl]sulfonyl}amino)phenyl]thio}benzoateHCID 11442458—

Reaktionsschritte

A solution of methyl 2-[(2-aminophenyl)thio]benzoate (0.444 g, 1.71 mmol) and 4-(acetylamino)benzenesulfonyl chloride (0.440 g, 1.88 mmol) in pyridine (1.6 mL) was stirred at room temperature for 1 hr. The reaction mixture was diluted with ethyl acetate and washed with 0.5 N HCl (×2), water (×2), half brine and brine. The organic layer was dried over sodium sulfate, filtered, and concentrated. The residue was purified by silica gel chromatography eluted with 1-5% MeOH in DCM to provide the title compound. MS (ES, M+H+): 457.2. 1H NMR (400 MHz, CD3OD) δ 7.92 (bd, J=8 Hz, 1H), 7.75 (bd, J=8 Hz, 1H), 7.55 (bd, J=9.2 Hz, 2H), 7.50-7.44 (m, 3H), 7.42 (bd, J=8 Hz, 1H), 7.18 (bt, J=7.6 Hz, 1H), 7.14 (bt, J=7.6 Hz, 1H), 7.05 (bt, J=8 Hz, 1H), 6.23 (bd, J=8 Hz, 1H), 3.95 (s, 3H), 2.14 (s, 3).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07393873B2
Quelldatensatzuspto-grants-2008_07
ORD IDord-02c64c4ec5bc4132bdd771d93dd44e68
Quellennotizuspto-grants-2008_07