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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989219Generated: October 30, 2026

5-Methoxy-6-(trifluoromethyl)indoline → HCID 10837468, compound

https://huagongshe.com/reaction/989219

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Methoxy-6-(trifluoromethyl)indolineHCID 11206713—
ReactantHCID 18005145HCID 18005145—
SolventDimethylformamideHCID 6228—
ProductHCID 10837468HCID 1083746826%

Reaction Steps

Phenyl N-[2,3-dihydro-7-(pyrid-3-yl)benzofuran-5-yl]carbamate (D65) (0.20 g, 0.00060 mole) in dry DMF (10 ml) was treated under argon with 5-methoxy-6-trifluoromethyl indoline (D11) (0.13 g, 0.00060 mole) and heated under reflux for 18 hours. The reaction was allowed to cool to ambient temperature and the solvent was removed in vacuo. The residue was dissolved in dichloromethane, washed with deionised water and 10% sodium hydroxide solution, dried (Na2SO4) and evaporated in vacuo. The resulting brown oil was purified by flash column chromatography on silica gel eluting with 2% methanol/dichloromethane, followed by recrystallisation from ethyl acetate 60.80° petroleum ether to afford the title compound (0.07 g, 26%) as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06638953B2
Source datasetuspto-grants-2003_10
ORD IDord-56e7dc40820441d6a59207a31ee01d62
Source noteuspto-grants-2003_10