HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496043Generated: October 31, 2026
Potassium Carbonate → HCID 10295642, compound
https://huagongshe.com/reaction/496043
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-fluoro-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole | HCID 11344959 | — |
| Reactant | HCID 12051141 | HCID 12051141 | — |
| Solvent | tetrahydrofuran N,N-dimethylformamide | HCID 21974620 | — |
| Product | HCID 10295642 | HCID 10295642 | — |
Reaction Steps
To a mixture of (2R)-2,3,8,9-tetrahydro-7H-[1,4]dioxino[2,3-h]chromen-2-ylmethyl 4-methylbenzenesulfonate (0.25 g, 0.66 mmole) and potassium carbonate (0.22 g, 1.55 mmole) in 1:1 tetrahydrofuran/dimethylformamide (20 mL) was added 0.45 g (2.08 mmole) of 5-fluoro-3-(1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole. The reaction mixture was refluxed under nitrogen for six hours. After completion, the mixture was evaporated to dryness under reduced pressure and the residue was column chromatographed on silica gel with methylene chloride to remove impurities and 4% methanol/methylene chloride to elute the desired product as an oil, which was crystallized from isopropanol with the addition of a solution of oxalic acid in hot isopropanol to give 0.040 g (6%) of the (S)-enantiomer of the title compound as a dark yellow solid, m.p. 146-148° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06943178B2 |
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| Source dataset | uspto-grants-2005_09 |
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| ORD ID | ord-6b8800fc16f4444abbbe8a38b2a73534 |
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| Source note | uspto-grants-2005_09 |
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