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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603807Generated: November 1, 2026

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

https://huagongshe.com/reaction/1603807

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, 0.00060mole) 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 numberUS05990133
Source datasetuspto-grants-1999_11
ORD IDord-5b68f605669e4833aec4f968db261665
Source noteuspto-grants-1999_11