HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → HCID 58541878, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-[1-tert-Butyl-2-(5-methoxy-2-pyrazol-1-yl-phenyl)-1H-benzimidazol-5-yl]-pyrimidin-2-ylamine | HCID 58541937 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58541878 | HCID 58541878 | 14% |
Reaction Steps
To a solution of 5-[1-tert-butyl-2-(5-methoxy-2-pyrazol-1-yl-phenyl)-1H-benzimidazol-5-yl]-pyrimidin-2-ylamine (Example 2) (75 mg, 0.17 mmol) in CH2Cl2 (10 mL) is added BBr3 (1M in THF) (0.5 mL, 0.51 mmol) at 0° C. under nitrogen atmosphere. The solution is warmed to room temperature and stirred for 48 hours. The solution is cooled down to 4° C. and saturated NaHCO3 solution (5 mL) is added. The mixture is extracted with EtOAc (3×10 mL) and the combined organic layer is dried (MgSO4), filtered and concentrated and the residue is purified by silica gel flash chromatography eluting with 10% MeOH in CH2Cl2 to afford the title compound (10 mg, 14%) as a white foam. LCMS (ESMS): m/z 426.20 (M++1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08420655B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-ec4ead4876e64fd3bd507beb12b332df |
| Source note | uspto-grants-2013_04 |