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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1936709Generated: October 27, 2026

1-Acetyl-7-(1-methyl-1,2,5,6-tetrahydropyridin-4-yl)-1,2,3,5-tetrahydropyrrolo [2,3-f]indole → 1-Acetyl-7-(1-methylpiperidin-4-yl)-1,2,3,5-tetrahydropyrrolo[2,3-f]indole

https://huagongshe.com/reaction/1936709

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Acetyl-7-(1-methyl-1,2,5,6-tetrahydropyridin-4-yl)-1,2,3,5-tetrahydropyrrolo [2,3-f]indoleHCID 22462530—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
Product1-Acetyl-7-(1-methylpiperidin-4-yl)-1,2,3,5-tetrahydropyrrolo[2,3-f]indoleHCID 22462547—

Reaction Steps

A mixture of 1-acetyl-7-(1-methyl-1,2,5,6-tetrahydropyridin-4-yl)-1,2,3,5-tetrahydropyrrolo[2,3-f]indole (D4, 1.10 g, 3.7 mmole), 10% palladium on carbon (0.20 g) in MeOH (50 ml), DMF (10 ml) and glacial acetic acid (0.5 ml) was shaken under hydrogen at 50 psi/344.8 kPa for 42 hours. The mixture was filtered through Celite (Diatomaceous Earth) and the filtrate evaporated to dryness. The residue was dissolved in water (10 ml) and the pH adjusted to 8 with solid potassium carbonate. The precipitate was collected by filtration washed with water and dried in vacuo to leave the title compound as a buff powder (0.60 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06391891B1
Source datasetuspto-grants-2002_05
ORD IDord-927204d0f0af4b5ba7f59af28c7918dc
Source noteuspto-grants-2002_05