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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357788Generated: November 2, 2026

5-fluoro-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole → HCID 10274376, compound

https://huagongshe.com/reaction/1357788

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-fluoro-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indoleHCID 11344959—
ReactantHCID 12083390HCID 12083390—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
ProductHCID 10274376HCID 10274376—

Reaction Steps

A solution of 0.41 g (0.1.1 mmole) of [(2R)-8-ethyl-2,3-dihydro-7H-[1,4]-dioxino[2,3-e]indol-2-yl]methyl 4-methylbenzenesulfonate and 0.71 g (3.3 mmole) of 5-fluoro-3-(1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole in 25 mL of DMSO were heated at 75-80° C. for 4 hours. The mixture was diluted with 300 mL of ethyl acetate, washed with 200 ml portions of saturated aqueous sodium bicarbonate and saturated brine, dried over magnesium sulfate, filtered and concentrated in vacuum. The residue was column chromatographed on silica gel with 0-2% methanol in methylene chloride as eluant. The product fractions were combined and concentrated in vacuum, and the residue triturated with ether/hexane (1:1) to give 0.090 g of the (S)-enantiomer of the title compound as a yellow solid hydrate, m.p. 81-82° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06593350B2
Source datasetuspto-grants-2003_07
ORD IDord-bc5baa8a926f469da540d4d80c705214
Source noteuspto-grants-2003_07