HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 59351479, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 59351757 | HCID 59351757 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59351479 | HCID 59351479 | 87% |
Reaction Steps
To a mixture of 4′-[(5-ethyl-2-oxo-1,2-dihydro-3H-thieno[2,3-d]imidazol-3-yl)methyl]biphenyl-2-carbonitrile (0.5 g), (2-bromoethyl)benzene (0.23 mL) and N,N-dimethylformamide (20 mL) was added 60% sodium hydride (0.066 g), and the mixture was stirred at room temperature for 2 hr. The reaction mixture was diluted with ethyl acetate, washed with 5% potassium hydrogensulfate and then saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to give the title compound as a colorless amorphous solid (0.58 g, 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08501750B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-dcce30b8867b47e2a85dad0a872900df |
| Source note | uspto-grants-2013_08 |