HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → [5-(1-Biphenyl-4-ylmethyl-6-chloro-5-iodo-1H-benzoimidazol-2-yloxy)-2-methyl-phenyl]-phosphonic acid diethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Diethyl 5-hydroxy-2-methylphenylphosphonate | HCID 57481474 | — |
| Reactant | 1-Biphenyl-4-ylmethyl-6-chloro-5-iodo-2-methanesulfonyl-1H-benzoimidazole | HCID 67377642 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | [5-(1-Biphenyl-4-ylmethyl-6-chloro-5-iodo-1H-benzoimidazol-2-yloxy)-2-methyl-phenyl]-phosphonic acid diethyl ester | HCID 86761791 | — |
Reaction Steps
To a solution of 1-biphenyl-4-ylmethyl-6-chloro-5-iodo-2-methanesulfonyl-1H-benzoimidazole (1.2 g, 2.3 mmol) in DMF (10 ml) at rt was added K2CO3 (635 mg, 4.6 mmol), followed by (5-hydroxy-2-methyl-phenyl)-phosphonic acid diethyl ester (630 mg, 2.6 mmol). The mixture was stirred overnight at rt. The solvent was then removed on a rotary evaporator. The resulting residue was partitioned between EtOAc and a solution of half-saturated ammonium chloride. The EtOAc layer was washed with H2O, brine, and then dried with MgSO4. After rotary evaporation, the residue was purified by flash chromatography (SiO2, 12 g). The title compound was eluted with a gradient up to 50% EtOAc in Hexane as a mixture of the two protected regioisomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08410284B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-63a648e8322049c5935b34662b69866e |
| Source note | uspto-grants-2013_04 |