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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-fluoro-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole | HCID 11344959 | — |
| Reactant | HCID 12083390 | HCID 12083390 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 10274376 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06593350B2 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-bc5baa8a926f469da540d4d80c705214 |
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| Source note | uspto-grants-2003_07 |
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