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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 11099Erstellt: 23. Oktober 2026

Anthranilic Acid → 2-{[3-(4-(2-Chlorophenyl)-9-hydroxy-1,3-dioxo-2,3-dihydropyrrolo[3,4-c]carbazol-6 (1H)-yl)propyl]amino}benzoic acid

https://huagongshe.com/de/reaction/11099

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAnthranilic AcidHCID 227—
Edukt6-(3-Bromopropyl)-4-(2-chlorophenyl)-9-hydroxypyrrolo[3,4-c]carbazole-1,3(2H,6H)-dioneHCID 21980512—
Produkt2-{[3-(4-(2-Chlorophenyl)-9-hydroxy-1,3-dioxo-2,3-dihydropyrrolo[3,4-c]carbazol-6 (1H)-yl)propyl]amino}benzoic acidHCID 6958398688%

Reaktionsschritte

Reaction of the bromide (58) prepared as described in example 172 with o-anthranilic acid using the procedure described in example 179 gave the aniline (60) (88%), mp 261–263° C. 1H NMR δ [(CD3)2SO] 11.05 (s, 1H), 9.38 (s, 1H), 8.39 (d, J=2.4 Hz, 1H), 7.76 (m, 1H), 7.75 (s, 1H), 7.59 (d, J=8.7 Hz, 1H), 7.55 (m, 1H), 7.46 (m, 1H), 7.40 (m, 1H), 7.33 (m, 1H), 7.27 (m, 1H), 7.12 (dd, J=8.7, 2.4 Hz, 1H), 6.59–6.50 (m, 2H), 4.57 (t, J=6.7 Hz, 2H), 3.22–3.10 (m, 2H), 2.15–2.05 (m, 2H). FABMS found M+: 541.1230, 539.1234. C30H22ClN3O5 requires 541.1218, 539.1248.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07094798B1
Quelldatensatzuspto-grants-2006_08
ORD IDord-b89c3cc6000840ceb21cafb05db13925
Quellennotizuspto-grants-2006_08