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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454554Generated: November 1, 2026

Quinone → HCID 178511962, compound

https://huagongshe.com/reaction/1454554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantQuinoneHCID 4650—
ReactantHCID 22556984HCID 22556984—
ReactantHCID 86607736HCID 86607736—
SolventMethanolHCID 887—
ProductHCID 178511962HCID 178511962—

Reaction Conditions

Temperature60 °C

Reaction Steps

1-tert-Butyl-3-[3′-formyl-6,2′-bis-(2-methoxyethoxymethoxy)-biphenyl-3-ylmethyl]-urea (0.6 g, 1.15 mmol), prepared as in Reference 19, diaminobenzamidine hydrochloride (0.3 g, 1.6 mmol) and 1,4-benzoquinone (0.124 g, 1.15 mmol) were combined in methanol (15 mL) and the mixture was heated at 60° C. and stirred for 2 hours. The mixture was cooled to room temperature and the solvent was removed by evaporation to yield 2-[5′-3-tert-butylureidomethyl)-2,2′- bis-(2-methoxyethoxymethoxy)-biphenyl-3-yl]-1H-benzoimidazole-5-carboxamidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07479502B2
Source datasetuspto-grants-2009_01
ORD IDord-3b55ea578aaf4140be25a9afac0a8d45
Source noteuspto-grants-2009_01