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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411596Generated: October 28, 2026

Methyl p-toluenesulfonate → HCID 10270884, compound

https://huagongshe.com/reaction/411596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl p-toluenesulfonateHCID 6645—
ReactantSodium BicarbonateHCID 516892—
Reactant3-(1,2,3,6-Tetrahydropyridin-4-yl)-1H-indoleHCID 2761023—
Reactanttetrahydrofuran N,N-dimethylformamideHCID 21974620—
ProductHCID 10270884HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06559169B2
Source datasetuspto-grants-2003_05
ORD IDord-c0f0e8b5cc704938806f6a9d75dcd1b8
Source noteuspto-grants-2003_05