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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 486157Erstellt: 25. Oktober 2026

1,1'-Carbonyldiimidazole → 3-(4-Chloro-2-thenoyl)-2-oxindole-1-carboxamide

https://huagongshe.com/reaction/486157

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,1'-CarbonyldiimidazoleHCID 68263—
EduktImidazolateHCID 3386966—
Edukt2-Oxindole-1-carboxamideHCID 11517274—
Edukt4-Chlorothiophene-2-carboxylic acidHCID 12290695—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-(4-Chloro-2-thenoyl)-2-oxindole-1-carboxamideHCID 9905174—

Reaktionsschritte

The title compound was prepared according to the procedure of Example 55. An 831 mg (5.11 mmole) portion of 4-chloro-2-thiophenecarboxylic acid (prepared according to Iriarte, J., et al., J. Het. Chem., 13, 393 (1976)) was combined with 897 mg (5.53 mmole) of 1,1'-carbonyldiimidazole in 5 ml of N,N-dimethylformamide and the intermediate imidazolide coupled directly with 750 mg (4.26 mmole) of 2-oxindole-1-carboxamide in the presence of 1.40 g (11.49 mmole) of 4-(N,N-dimethylamino)pyridine. The resulting crude yellow solid (803 mg, 59% yield) was recrystallized from acetic acid to furnish 376 mg (1.17 mmole, 27% yield) of fluffy yellow crystals, m.p. 221°-3° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05290802
Quelldatensatzuspto-grants-1994_03
ORD IDord-324403d442e54561acf727dc10d64a3f
Quellennotizuspto-grants-1994_03