HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(benzyloxymethyl)-1H-tetrazole → 4-((1-(benzyloxymethyl)-1H-tetrazol-5-yl)(5-ethoxy-2-fluoro-3-isopropoxyphenyl)methylamino)benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(benzyloxymethyl)-1H-tetrazole | HCID 10631524 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178466720 | HCID 178466720 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-((1-(benzyloxymethyl)-1H-tetrazol-5-yl)(5-ethoxy-2-fluoro-3-isopropoxyphenyl)methylamino)benzonitrile | HCID 68816258 | 24.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07576098B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-3e94b99a5adc492fbcab42fc6c24c872 |
| Source note | uspto-grants-2009_08 |