HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron trifluoride etherate → HCID 178427329, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | HCID 86701683 | HCID 86701683 | — |
| Reactant | HCID 86701684 | HCID 86701684 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 178427329 | HCID 178427329 | — |
Reaction Steps
To a solution of a mixture of 2-((7-(hydroxymethyl)-5-methyl-1-tosyl-1H-indol-4-yl)methyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-benzo[d]imidazole-5-carbonitrile and 2-((7-(hydroxymethyl)-5-methyl-1-tosyl-1H-indol-4-yl)methyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-benzo[d]imidazole-6-carbonitrile (14 mg, 0.023 mmol) in DCM (0.23 mL), BF3.OEt2 (15 μL, 0.117 mmol) was added at 0° C. After stirring for 5 minutes, the mixture was warmed up to room temperature. After 30 minutes the reaction mixture was diluted with sat. aq. NaHCO3 and EtOAc, extracted with EtOAc, and the organic extract was dried over MgSO4, filtered and concentrated to provide the title compound, which was used without further purification. MS (ESI+) m/z 471.2 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09056874B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-534c8b7a4fe447a5b73d212d079336d1 |
| Source note | uspto-grants-2015_06 |