HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trityl chloride → HCID 86647616, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | HCID 86647615 | HCID 86647615 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86647616 | HCID 86647616 | 40% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Crude N-[5-(3,5-difluoro-benzyl)-1H-indazol-3-yl]-2,2,2-trifluoro-acetamide was suspended in dichloromethane (25 mL) and treated with trityl chloride (0.72 g, 2.58 mmol) under stirring. The suspension was cooled to 0° C. and neat 1,8-diazabicyclo[5.4.0]undec-7-ene (0.42 mL, 2.78 mmol) was added, producing immediate solubilization. After stirring at 0° C. for 3 hours the reaction mixture was poured into 50 mL of ice containing 1N HCl (5 mL) and extracted with dichloromethane. The organic layer was washed with NaHCO3, brine, dried and concentrated to a crude material that was purified by flash chromatography (eluant: DCM). The desired product was obtained as a white solid (450 mg, yield 40% over two steps)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09102662B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-584a75c5da574572b88df55f7aaea2e0 |
| Source note | uspto-grants-2015_08 |