HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromo-6-chloroquinoline → 4-((6-Chloroquinolin-2-yl)(5-ethoxy-2-fluoro-3-isopropoxyphenyl)methylamino)benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromo-6-chloroquinoline | HCID 17933523 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178466720 | HCID 178466720 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-((6-Chloroquinolin-2-yl)(5-ethoxy-2-fluoro-3-isopropoxyphenyl)methylamino)benzonitrile | HCID 68816823 | 55.5% |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
To a solution of Intermediate 90.1 (100 mg, 0.412 mmol) in 2 mL THF at −78° C., was added BuLi (1.4 M in hexanes, 324 μL, 0.454 mmol). The mixture was stirred at −78° C. for 10 min, then a solution of Intermediate 7.3 (134 mg, 0.412 mmol) in 0.7 mL THF was added. The mixture was stirred 15 min at −78° C., allowed to warm to rt over 30 min, then was quenched with sat. NH4Cl and diluted with EtOAc. The organic phase was washed with H2O and brine, dried (Na2SO4) and concentrated. The crude product was purified by flash chromatography (0 to 30% EtOAc/hexanes gradient) to afford 112 mg of Intermediate 90.2 as a pale orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07576098B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-16f243183ca04a0c88f82602f26104ca |
| Source note | uspto-grants-2009_08 |