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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647004Generated: October 30, 2026

4-Fluoro-3-methylbenzene-1,2-diamine → HCID 178429740, compound

https://huagongshe.com/reaction/647004

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluoro-3-methylbenzene-1,2-diamineHCID 22055547—
Reactant3-[3-(1-Methyl-piperidin-4-yloxy)-propoxy]-benzaldehydeHCID 57480931—
SolventDimethylformamideHCID 6228—
ProductHCID 178429740HCID 17842974037.8%

Reaction Steps

6-Fluoro-7-methyl-2-{3-[3-(1-methyl-piperidin-4-yloxy)-propoxy]-phenyl}-1H-benzoimidazole. To a stirred solution of 3-[3-(1-methyl-piperidin-4-yloxy)-propoxy]-benzonitrile (0187 g, 0.68 mmol, 1.0 equiv) in toluene (5.0 mL) at 0° C. was added 1.5 M diisobutylaluminum hydride in toluene (1.02 mL, 1.02 mmol, 1.5 equiv). After 3 h, methanol (9 mL) and 1 M H2SO4 (10 mL) were added. The mixture was stirred for 30 min, then 1.0 M NaOH (10 mL) was added, followed by satd. aq. sodium potassium tartrate (40 mL) and dichloromethane (100 mL). After stirring for 30 min, the mixture was extracted three times with chloroform (50 mL) and the combined extracts were washed with brine, dried (Na2SO4), filtered, and concentrated. The residue was partially purified by Method 2 to afford 106 mg of a mixture of 3-[3-(1-methyl-piperidin-4-yloxy)-propoxy]-benzaldehyde and several other unidentified products. A solution of the crude 3-[3-(1-methyl-piperidin-4-yloxy)-propoxy]-benzaldehyde (53 mg), 4-fluoro-3-methyl-benzene-1,2-diamine (27 mg), and Na2S2O5 in DMF was stirred at 90° C. for 18 h. The reaction mixture was loaded directly on silica gel and purified according to Method 2, which afforded 28.7 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07705143B2
Source datasetuspto-grants-2010_04
ORD IDord-f105f4d90244461891fc9b34b384c419
Source noteuspto-grants-2010_04