HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → [5-(1-Benzyl-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-Benzyl-6-chloro-5-iodo-2-methanesulfonyl-1H-benzoimidazole | HCID 67446146 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | [5-(1-Benzyl-6-chloro-5-iodo-1H-benzoimidazol-2-yloxy)-2-methyl-phenyl]-phosphonic acid diethyl ester | HCID 86761793 | — |
Reaction Steps
To a solution of 1-benzyl-6-chloro-5-iodo-2-methanesulfonyl-1H-benzoimidazole (2.7 g, 6.0 mmol) in DMF (30 ml) was added (5-hydroxy-2-methyl-phenyl)-phosphonic acid diethyl ester (1.9 g, 8.4 mmol), followed by potassium carbonate (1.7 g, 12 mmol). After stirring overnight at rt the volatiles were removed by rotary evaporation. The residue thus obtained was partitioned between EtOAc and half-saturated ammonium chloride solution. The EtOAc layer was washed with H2O, brine, and then dried with MgSO4. The crude oil was then purified by flash chromatrography (SiO2, 80 g) using a gradient up to 65% EtOAc in hexane to yield the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08410284B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-bf254ef767b24e67b28d758056d59f1f |
| Source note | uspto-grants-2013_04 |