Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Quinone | HCID 4650 | — |
| Reactant | 3,4-Diaminobenzimidamide | HCID 10975664 | — |
| Reactant | N-acetyl 5-formyl-6-hydroxy-biphenyl-3,3'-disulfonamide | HCID 86607737 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178475152 | HCID 178475152 | 14% |
Reaction Steps
N-acetyl 5-formyl-6-hydroxy-biphenyl-3,3′-disulfonamide (74 mg, 0.19 mmol) was dissolved in methanol (10 mL) and stirred at room temperature. 3,4-Diaminobenzamidine (39 mg, 0.21 mmol) and 1,4-benzoquinone (20 mg, 0.2 mmol) were added to the solution and the mixture was refluxed for 1 hour. The solvent was removed by rotary evaporation under reduced pressure and the residue was dissolved in water and acetonitrile and purified by reverse phase HPLC (0.02N HCl/ACN) to give 2-(5-acetylsulfamoyl-2-hydroxy-3′-sulfamoyl-biphenyl-3-yl)-1H-benzoimidazole-5-carboxamidine (14.1 mg) as a yellow amorphous powder. MS m/z: 527.4 (M−H+) and 529.3 (M+H+). 1H NMR (400 MHz, DMSO-d6): δ 9.36 (bs, 2H), 8.94 (bs, 2H), 8.08 (d, J=2.2 Hz, 1H), 8.22 (bs, 1H), 8.10 (t, J=1.5 Hz, 1H), 7.96 (d, J=2.2 Hz, 1H) 7.89 (d, J=1.8 Hz, 1H), 7.87-7.85 (m, 2H), 7.76 (dd, J=10, 1.5 Hz, 1H), 7.71 (t, J=7.7 Hz, 1H), 7.46 (s, 2H) and 1.96 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09162986B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-8d697d50e7794a48970e9c29251be164 |
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| Source note | uspto-grants-2015_10 |
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