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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168708Generated: October 28, 2026

5-fluoro-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole → HCID 9887424, compound

https://huagongshe.com/reaction/1168708

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-fluoro-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indoleHCID 11344959—
ReactantHCID 12083387HCID 12083387—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
ProductHCID 9887424HCID 9887424—

Reaction Steps

A solution of 0.30 g (0.84 mmole) of (2R)-2,3-dihydro-7H-[1,4]dioxino[2,3-e]indol-2-ylmethyl 4-methylbenzenesulfonate and 0.40 g (1.8 mmole) of 5-fluoro-3-(1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole in 30 mL of DMSO was heated at 65° 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 0-1.5% 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 0.10 g of the (S)-enantiomer of the title compound as a yellow solid, m.p. 112° C., with one-quarter mole of ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06627639B2
Source datasetuspto-grants-2003_09
ORD IDord-14b9de7a8e274eb4823acd77e721acab
Source noteuspto-grants-2003_09