Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646959Generated: October 27, 2026

3,4-Dimethylbenzene-1,2-diamine → 4,5-Dimethyl-2-{3-methyl-4-[3-(4-methyl-piperazin-1-yl)-propoxy]-phenyl}-1H-benzoimidazole

https://huagongshe.com/reaction/646959

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dimethylbenzene-1,2-diamineHCID 521077—
Reactant3-Methyl-4-[3-(4-methylpiperazin-1-yl)propoxy]benzaldehydeHCID 57525427—
Product4,5-Dimethyl-2-{3-methyl-4-[3-(4-methyl-piperazin-1-yl)-propoxy]-phenyl}-1H-benzoimidazoleHCID 1174970275.3%

Reaction Steps

This compound was prepared by the method described in Example 1, using 3-methyl-4-[3-(4-methyl-piperazin-1-yl)-propoxy]-benzaldehyde (180 mg, 0.65 mmol, 1.0 equiv), 3,4-dimethyl-benzene-1,2-diamine (89 mg, 0.65 mmol, 1.0 equiv), and Na2S2O5 (161 mg, 0.85 mmol, 1.3 equiv) in General Procedure 3. Purification by Method 2 afforded 192 mg (75%) of the title compound. MS (electrospray): mass calculated for C24H32N4O, 392.26. m/z found, 393.5 [M+H]+. 1H NMR (400 MHz, CD3OD): 7.95-7.85 (m, 2H), 7.35-7.23 (m, 1H), 7.08-7.00 (m, 2H), 4.12 (t, J=6.0 Hz, 2H), 2.64-2.37 (m, 16H), 2.29 (s, 6H), 2.10-2.00 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07705149B2
Source datasetuspto-grants-2010_04
ORD IDord-cb68af327cb446ba815ba5bd79be1208
Source noteuspto-grants-2010_04