Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Quinone | HCID 4650 | — |
| Reactant | HCID 22556984 | HCID 22556984 | — |
| Reactant | HCID 86607736 | HCID 86607736 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178511962 | HCID 178511962 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07479502B2 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-3b55ea578aaf4140be25a9afac0a8d45 |
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| Source note | uspto-grants-2009_01 |
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