HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411596Generated: October 28, 2026
Methyl p-toluenesulfonate → HCID 10270884, compound
https://huagongshe.com/reaction/411596
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl p-toluenesulfonate | HCID 6645 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-(1,2,3,6-Tetrahydropyridin-4-yl)-1H-indole | HCID 2761023 | — |
| Reactant | tetrahydrofuran N,N-dimethylformamide | HCID 21974620 | — |
| Product | HCID 10270884 | HCID 10270884 | — |
Reaction Steps
(2R)-8-Methoxy-2,3-dihydro-benzo[1,4]dioxin-2-yl]methyl-4-methylbenzenesulfonate (1.1 g, 3.1 mmole) was dissolved in a mixture of dimethylformamide/tetrahydrofuran (1:1 v/v, 50 mL) and 3-(1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole (0.60 g 1.6 mmole) added, followed by sodium bicarbonate (1.0 g). The reaction mixture was refluxed under nitrogen for 18 hours, then cooled and concentrated in vacuum. The residue was partitioned between 400 mL each of water and ethyl acetate. The layers were separated. The organic phase was washed with water and saturated aqueous sodium chloride solution, dried over anhydrous potassium carbonate and evaporated to a foam (1.0 g). Trituration with ether yielded a solid which was recrystallized from boiling chloroform/methanol (1:1 v/v) to give 0.40 g (40%) of the (S)-enantiomer of the title compound as an off-white solid one-quarter hydrate, m.p. 203-205° 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-c0f0e8b5cc704938806f6a9d75dcd1b8 |
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| Source note | uspto-grants-2003_05 |
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