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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2105049생성일: 2026년 10월 24일

1-Methyl-3-phenyl-1H-1,2,4-triazole → (3-(tert-butyldimethylsilyloxy)-5-ethyl-2-fluorophenyl)(2-methyl-5-phenyl-2H-1,2,4-triazol-3-yl)methanol

https://huagongshe.com/ko/reaction/2105049

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참여 물질

역할이름HCID투입량
반응물1-Methyl-3-phenyl-1H-1,2,4-triazoleHCID 10877408—
반응물3-{[tert-Butyl(dimethyl)silyl]oxy}-5-ethyl-2-fluorobenzaldehydeHCID 59838072—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물(3-(tert-butyldimethylsilyloxy)-5-ethyl-2-fluorophenyl)(2-methyl-5-phenyl-2H-1,2,4-triazol-3-yl)methanolHCID 5780401156.3%

반응 조건

온도23 °C

반응 단계

To a solution of 1-methyl-3-phenyl-1H-1,2,4-triazole (310 mg, 1.95 mmol, see J. Chem. Soc., 1954, 3319-3322) in THF (25 mL) cooled to −78° C. was added 1.6 M n-butyl lithium (1.33 mL, 2.12 mmol) dropwise and stirred for 15 min. Next a solution of Intermediate 368.2 (500 mg, 1.77 mmol) in THF (5 mL) was added dropwise and stirred for 5 min before allowing the mixture to warm to 23° C. The mixture was quenched with aqueous NH4Cl and extracted with EtOAc (3×50 mL). The organic layer was washed with H2O, brine, dried (Na2SO4) and concentrated. The crude product was purified by flash chromatography (0 to 60% EtOAc/hexanes gradient) to afford 440 mg of Example 368.3. HPLC (2 min gradient) RT=2.42 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07576098B2
출처 데이터셋uspto-grants-2009_08
ORD IDord-2bfddfb368cc4fb48a37f28e0faafdbc
출처 메모uspto-grants-2009_08