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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104953Generated: October 30, 2026

1-(benzyloxymethyl)-1H-tetrazole → 4-((1-(benzyloxymethyl)-1H-tetrazol-5-yl)(5-ethoxy-2-fluoro-3-isopropoxyphenyl)methylamino)benzonitrile

https://huagongshe.com/reaction/2104953

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(benzyloxymethyl)-1H-tetrazoleHCID 10631524—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178466720HCID 178466720—
SolventTetrahydrofuranHCID 8028—
Product4-((1-(benzyloxymethyl)-1H-tetrazol-5-yl)(5-ethoxy-2-fluoro-3-isopropoxyphenyl)methylamino)benzonitrileHCID 6881625824.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of Intermediate 12.1 (50.0 mg, 0.263 mmol) in 2 mL THF at −78° C. was added 1.6 M solution of BuLi in THF (181 μL, 0.289 mmol). The mixture was stirred at −78° C. for 2 min, then a solution of Intermediate 7.3 (86 mg, 0.263 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 (25 to 30% EtOAc/hexanes, stepwise gradient) to afford 33 mg of Intermediate 12.2 as yellow residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576098B2
Source datasetuspto-grants-2009_08
ORD IDord-3e94b99a5adc492fbcab42fc6c24c872
Source noteuspto-grants-2009_08