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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104975Generated: October 30, 2026

2-Bromo-6-chloroquinoline → 4-((6-Chloroquinolin-2-yl)(5-ethoxy-2-fluoro-3-isopropoxyphenyl)methylamino)benzonitrile

https://huagongshe.com/reaction/2104975

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-6-chloroquinolineHCID 17933523—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178466720HCID 178466720—
SolventTetrahydrofuranHCID 8028—
Product4-((6-Chloroquinolin-2-yl)(5-ethoxy-2-fluoro-3-isopropoxyphenyl)methylamino)benzonitrileHCID 6881682355.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576098B2
Source datasetuspto-grants-2009_08
ORD IDord-16f243183ca04a0c88f82602f26104ca
Source noteuspto-grants-2009_08