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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1278723Generated: November 1, 2026

2,3-Dimethyl-5,6-diamino-1,4-dimethoxybenzene → 2-[2-(3,4-Dimethoxyphenyl)-vinyl]-4,7-dimethoxy-5,6-dimethyl-1H-benzoimidazole

https://huagongshe.com/reaction/1278723

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dimethyl-5,6-diamino-1,4-dimethoxybenzeneHCID 18431172—
ReactantMethyl-(3,4-dimethoxy)-cinnamoimidate hydrochlorideHCID 86758495—
SolventMethanolHCID 887—
Product2-[2-(3,4-Dimethoxyphenyl)-vinyl]-4,7-dimethoxy-5,6-dimethyl-1H-benzoimidazoleHCID 5402578558%

Reaction Steps

A mixture of 2,3-dimethyl-5,6-diamino-1,4-dimethoxybenzene (2.57 g; 10 mmol) and methyl-(3,4-dimethoxy)-cinnamoimidate hydrochloride (1.96 g; 10 mmol) in methanol (35 mL) was stirred at ambient temperature for 18 hours. The methanol solution was concentrated to 15 mL. The yellow precipitate was separated by filtration. Recrystallization from MeOH afforded 2.1 g (58% yield) of the title compound as yellow solid, m.p. 116-119° C. Anal. Calcd. for C21H24N2O4: C, 66.46, H, 6.57; N, 7.60. Found: C, 66.83; H, 6.64; N, 7.41. Mass spectrum: (EI,M+) m/z 368 1H-NMR (DMSO-d6; 400 MHz) δ12.4-12.5(broad s,1H), 7.6-7.4 (d, 1H), 7.2 (d, 1H), 7.07-7.16 (m, 2H), 7.0 (d, 1H), 3.84(s, 3H), 3.78 (s, 3H), 2.2 ppm (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06444694B1
Source datasetuspto-grants-2002_09
ORD IDord-2f6a074a9a434532b2bccddf882caf0c
Source noteuspto-grants-2002_09