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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706312Generated: October 30, 2026

1,1'-Carbonyldiimidazole → HCID 178488769, compound

https://huagongshe.com/reaction/706312

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant2,4-DimethoxybenzaldehydeHCID 69175—
ReactantTrimethylsilyl cyanideHCID 82115—
ReactantHCID 178507353HCID 178507353—
CatalystPalladiumHCID 23938—
ProductHCID 178488769HCID 17848876930%

Reaction Steps

The compound was synthesized starting from 1H-benzo[d]imidazol-5-amine (0.400 g, 3 mmol), 2,4-dimethoxybenzaldehyde (0.5 g, 3 mmol), TMSCN (0.375 mL, 3 mmol), Pd/C (10%, 0.02 g), TEA 1.05 mL, 7.5 mmol), di-(imidazol-1-yl)methanone (0.730 g, 4.5 mmol) as described in method 2 to give 1-(1H-benzo[d]imidazol-5-yl)-5-(2,4-dimethoxyphenyl)imidazolidin-2-one (yield: 0.305 g, 0.9 mmol, 30%). Treating with borontribromide (0.512 mL, 5.41 mmol) as described for Example 151 gives the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09173885B2
Source datasetuspto-grants-2015_11
ORD IDord-430156390e8944e9a2eb2bf86f98e265
Source noteuspto-grants-2015_11