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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-Methyl-3-phenyl-1H-1,2,4-triazole | HCID 10877408 | — |
| 반응물 | 3-{[tert-Butyl(dimethyl)silyl]oxy}-5-ethyl-2-fluorobenzaldehyde | HCID 59838072 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (3-(tert-butyldimethylsilyloxy)-5-ethyl-2-fluorophenyl)(2-methyl-5-phenyl-2H-1,2,4-triazol-3-yl)methanol | HCID 57804011 | 56.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07576098B2 |
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| 출처 데이터셋 | uspto-grants-2009_08 |
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| ORD ID | ord-2bfddfb368cc4fb48a37f28e0faafdbc |
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| 출처 메모 | uspto-grants-2009_08 |
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