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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361238Generated: November 1, 2026

4-(3-(1-(2-Fluorophenyl)-2-nitroethyl)-1H-indol-6-yl)morpholine → 2-(2-Fluorophenyl)-2-(6-morpholino-1H-indol-3-yl)ethanamine

https://huagongshe.com/reaction/2361238

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(3-(1-(2-Fluorophenyl)-2-nitroethyl)-1H-indol-6-yl)morpholineHCID 67994905—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
Product2-(2-Fluorophenyl)-2-(6-morpholino-1H-indol-3-yl)ethanamineHCID 6799479184%

Reaction Steps

A mixture of 4-(3-(1-(2-fluorophenyl)-2-nitroethyl)-1H-indol-6-yl)morpholine (0.235 g, 0.636 mmol) and Raney Ni (a small spatula) in MeOH (30 mL) was treated with hydrogen at 55 psi in a Parr shaker apparatus for 3 hr. The catalyst was removed by suction filtration. The filtrate was concentrated under vacuum, diluted with CH2Cl2 (100 mL), washed with brine (25 mL) and dried over anhydrous MgSO4. Removal of solvent under vacuum provided the desired product (0.181 g, 0.533 mmol, 84% yield) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685969B2
Source datasetuspto-grants-2014_04
ORD IDord-e2dc87c02179445f8bf313f88df01143
Source noteuspto-grants-2014_04