Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843939Generated: October 29, 2026

Potassium Carbonate → 6-benzyloxy-3-(propyl)amino-1,2,3,4-tetrahydro-9H-carbazole

https://huagongshe.com/reaction/843939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-IodopropaneHCID 33643—
Reactant6-benzyloxy-3-amino-1,2,3,4-tetrahydro-9H-carbazoleHCID 22611308—
SolventAcetonitrileHCID 6342—
Product6-benzyloxy-3-(propyl)amino-1,2,3,4-tetrahydro-9H-carbazoleHCID 2261139039.4%

Reaction Steps

To a solution of 0.600 gm (2.05 mMol) 6-benzyloxy-3-amino-1,2,3,4-tetrahydro-9H-carbazole in 35 mL acetonitrile were added 0.283 gm (2.05 mMol) potassium carbonate followed by 240 μL (2.46 mMol) iodopropane and the reaction mixture was stirred at room temperature for 2.5 days. Additional iodopropane was added and the reaction stirred at room temperature until all of the starting material had been consumed. The reaction mixture was then partitioned between dichloromethane and water. The aqueous phase was extracted with dichloromethane and the combined organic phases were then dried over magnesium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel chromatography, eluting with 96.5:3:0.5 dichloromethane: isopropanol:ammonium hydroxide. Fractions shown to contain the desired compound were concentrated under reduced pressure to give 0.270 gm (39%) of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06380201B1
Source datasetuspto-grants-2002_04
ORD IDord-2a44b651a3d54f439bfa68543c8574c7
Source noteuspto-grants-2002_04