HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrabutylammonium Fluoride → HCID 178480026, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | (Rac)-[6-(1-methyl-1h-pyrazol-4-yl)-imidazo[1,2-b]pyridazin-3-yl]-[1-(2-trimethylsilanyl-ethoxymethyl)-1h-benzoimidazol-5-yl]-methanol | HCID 68640134 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178480026 | HCID 178480026 | — |
Reaction Steps
TBAF (1 M, 200 uL) was added to (rac)-[6-(1-Methyl-1H-pyrazol-4-yl)-imidazo[1,2-b]pyridazin-3-yl]-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-benzoimidazol-5-yl]-methanol (Stage 162.2, 42 mg, 0.088 mmol) dissolved in THF (3 ml). The reaction mixture was heated at reflux for 1 h. After evaporation of the solvent, the residue was taken into EtOAc and washed with saturated aqueous sodium carbonate. The aqueous phase was again extracted with EtOAc (3×) and combined organic layers were dried on Na2SO4. After evaporation of the solvent, the title compound was obtained as an oil (tR 0.01 min (conditions 2), MH+=346).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08822468B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-554d3d8133974513be7f0c5057ed1cae |
| Source note | uspto-grants-2014_09 |