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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278022Generated: October 26, 2026

4-Fluorobenzene-1,2-diamine → 5-(5-Fluorobenzimidazol-2-yl)-3-(1-Methylpiperidin-4-yl)-1H-Indole

https://huagongshe.com/reaction/278022

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzene-1,2-diamineHCID 164584—
Reactant5-Formyl-3-(1-Methylpiperidin-4-yl)-1H-IndoleHCID 22626786—
SolventNitrobenzeneHCID 7416—
Product5-(5-Fluorobenzimidazol-2-yl)-3-(1-Methylpiperidin-4-yl)-1H-IndoleHCID 1204181125%

Reaction Conditions

Temperature155 °C

Reaction Steps

A solution of 5-formyl-3-(1-methylpiperidin-4-yl)-1H-indole (0.210 g, 0.90 mmol), and 4-fluoro-o-phenylenediamine (0.112 g, 0.90 mmol), in 15 mL of nitrobenzene was heated, with stirring, at 150-160° C. for 24 hours. An additional 0.5 equivalents of the diamine was added, and heating continued for an additional 24 hours. The solution was allowed to cool to room temperature, the solvent was removed in vacuo, and the residue was purified by silica gel chromatography (dichloromethane:methanol 10:1.5) to give the title compound (0.075 g, 25%) as an amorphous tan solid. FDMS m/e=348 (M+). EA calculated for C21H21N4F.¾ H2O: C, 69.69; H, 6.27; N, 15.48. Found: C, 69.61; H, 6.19; N, 15.17.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06358972B1
Source datasetuspto-grants-2002_03
ORD IDord-d4fb135a88004116a74448d718e06f2c
Source noteuspto-grants-2002_03