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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603759Generated: November 1, 2026

Water → 1-(3-Fluoro-5-iodophenylcarbamoyl)-5-methoxy-6-trifluoromethylindoline

https://huagongshe.com/reaction/1603759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant3-Fluoro-5-iodoanilineHCID 2758986—
Reactant5-Methoxy-6-(trifluoromethyl)indolineHCID 11206713—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product1-(3-Fluoro-5-iodophenylcarbamoyl)-5-methoxy-6-trifluoromethylindolineHCID 1800514340%

Reaction Steps

A mixture of 3-fluoro-5-iodoaniline (0.47 g, 1.98 mmol) and 1,1'-carbonyl diimidazole (0.33 g, 2 mmol) in dichloromethane (40 ml) was stirred at room temperature for 1 h, then evaporated to dryness. To the residue was added dimethylformamide (DMF,10 ml) and a solution of 5-methoxy-6-trifluoromethylindoline (D11, 0.44 g, 2 mmol) in DMF (5 ml). The mixture was heated at 80° C. overnight, then cooled and poured into water. The precipitate was filtered off, washed with water and dried. The crude product was chromatographed on silica gel and eluted with dichloromethane. Eluted product was recrystallised from dichloromethane to give tie title compound (0.38 g, 40%), Mp. 221-4° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990133
Source datasetuspto-grants-1999_11
ORD IDord-de35233a49f0451b9bfb7ff00649797e
Source noteuspto-grants-1999_11