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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104951Generated: November 1, 2026

1-benzyloxymethyl-1H-benzimidazole → 4-((1-(benzyloxymethyl)-1H-benzo[d]imidazol-2-yl)(5-ethoxy-2-fluoro-3-isopropoxyphenyl)methylamino)benzonitrile

https://huagongshe.com/reaction/2104951

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-benzyloxymethyl-1H-benzimidazoleHCID 11322375—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178466720HCID 178466720—
SolventTetrahydrofuranHCID 8028—
Product4-((1-(benzyloxymethyl)-1H-benzo[d]imidazol-2-yl)(5-ethoxy-2-fluoro-3-isopropoxyphenyl)methylamino)benzonitrileHCID 6881377080.1%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of Intermediate 10.1 (50.0 mg, 0.210 mmol) in 2 mL THF at −78° C. was added 1.6 M solution of BuLi in THF (144 μL, 0.231 mmol). The mixture was stirred at −78° C. for 15 min, then a solution of Intermediate 7.3 (69 mg, 0.210 mmol) in 0.6 mL THF was added dropwise. The mixture was stirred at −78° C. for 30 min, was allowed to warm to rt over 1 h, then was quenched with sat. NH4Cl. The mixture was diluted with EtOAc, washed with H2O and brine, dried (Na2SO4) and concentrated. The crude product was purified by flash chromatography (0 to 40% EtOAc/hexanes gradient) to afford 95 mg of Intermediate 10.2 as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576098B2
Source datasetuspto-grants-2009_08
ORD IDord-3fbdc59e942440f0ba4207a869cc4fd1
Source noteuspto-grants-2009_08