HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411600Generated: October 30, 2026
Sodium Bicarbonate → HCID 10177548, compound
https://huagongshe.com/reaction/411600
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-(1,2,3,6-Tetrahydropyridin-4-yl)-1H-indole | HCID 2761023 | — |
| Reactant | HCID 11792132 | HCID 11792132 | — |
| Solvent | tetrahydrofuran N,N-dimethylformamide | HCID 21974620 | — |
| Product | HCID 10177548 | HCID 10177548 | — |
Reaction Steps
[(2R)-7-Methoxy-2,3-dihydro-benzo[1,4]dioxin-2-yl]methyl 4-methylbenzenesulfonate (1.5 g, 4.3 mmole) was dissolved in a mixture of dimethylformamide/tetrahydrofuran (1:1 v/v, 30 mL) and 3-(1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole (0.80 g, 4.0 mmole) added, followed by sodium bicarbonate (1.0 g), and the mixture was refluxed under nitrogen for 18 hours. The solvent was removed under vacuum and the residue partitioned between 400 mL each of methylene chloride and water. The layers were separated and the organic phase was washed with water and saturated sodium chloride solution, dried over potassium carbonate and filtered. The filtrate was evaporated to a foam (1.6 g). Chromatography on silica gel using 4% methanol in chloroform as eluant gave 0.20 g of the (S)-enantiomer of the title compound as a yellow solid, m.p. 166-168° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06559169B2 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-68bc75c5f44d4b6799b87c78322e1a02 |
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| Source note | uspto-grants-2003_05 |
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