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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277991Generated: October 25, 2026

5-Methoxy-3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole → 5-methoxy-3-(1-methylpiperidin-4-yl)-1H-indole

https://huagongshe.com/reaction/277991

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Methoxy-3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indoleHCID 3055249—
CatalystPalladiumHCID 23938—
SolventEthanol tetrahydrofuran methanolHCID 66624091—
Product5-methoxy-3-(1-methylpiperidin-4-yl)-1H-indoleHCID 1137956197.2%

Reaction Steps

5-Methoxy-3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)indole (9.00 g, 37 mmol) was dissolved in 190 mL of ethanol/tetrahydrofuran/methanol (10:10:1). 10% palladium on carbon (2.2 g) was added, and the reaction mixture was hydrogenated at 40 p.s.i. in a Parr shaker for 96 hours. The mixture was filtered through celite, the catalyst was washed with ethanol, and the filtrate was concentrated in vacuo. The residue was chromatographed on silica gel (5-10% 2M ammonia-methanol/dichloromethane) to provide 8.79 g (97%) of the title compound. MS(m/e): 245 (M+). EA calculated for C14H19N3O: C, 68.54; H, 7.81; N, 17.13. Found: C, 68.40; H, 7.52; N, 16.90.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06358972B1
Source datasetuspto-grants-2002_03
ORD IDord-51bbd5a46bc34511b3c13486cdf4eccd
Source noteuspto-grants-2002_03