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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167375Generated: October 31, 2026

5-fluoro-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole → HCID 10140200, compound

https://huagongshe.com/reaction/1167375

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-fluoro-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indoleHCID 11344959—
ReactantHCID 12082523HCID 12082523—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
ProductHCID 10140200HCID 10140200—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of (2R)-8,9-diethyl-2,3-dihydro[1,4]dioxino[2,3-f]-quinoxalin-2-ylmethyl 4-methylbenzenesulfonate (0.300 g, 0.700 mmole) in methyl sulfoxide (20 mL) was added 5-fluoro-3-(1,2,3,6-tetrahydro-4-pyridinyl)-1 H-indole (0.606 g, 2.800 mmole) and the reaction mixture was heated to 80° C. for 12 hours. The reaction mixture was allowed to cool to room temperature and was diluted with ethyl acetate (250 mL), washed with water (2×100 mL), aqueous sodium chloride (100 mL), dried (magnesium sulfate) and the solvent was removed in vacuo to give a crude solid. Purification by flash column chromatography (silica, methanol:ethyl acetate 1:9) followed by recrystallization from ethanol provided 0.161 g (49%) of the (S)-enantiomer of the title compound as a yellow crystalline solid. Rf =0.38 (silica, methanol:ethyl acetate 1:9); mp>120° C. dec.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06617327B2
Source datasetuspto-grants-2003_09
ORD IDord-c492ae8b639c415a8a145de931f8647a
Source noteuspto-grants-2003_09