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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 60644생성일: 2026년 10월 25일

Potassium Carbonate → 3-(5-Amino-3-tert-butyl-pyrazol-1-yl)-5-methyl-phenol

https://huagongshe.com/reaction/60644

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물(1R,2R)-N1,N1-Dimethylcyclohexane-1,2-diamineHCID 11275066—
반응물3-Bromo-5-methylphenolHCID 12648409—
반응물HCID 178441179HCID 178441179—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
생성물3-(5-Amino-3-tert-butyl-pyrazol-1-yl)-5-methyl-phenolHCID 11772958749.2%

반응 조건

온도140 °C

반응 단계

5-tert-Butyl-2H-pyrazol-3-ylamine (1.11 g, 8.00 mmol), potassium carbonate (2.32 g, 16.8 mmol), copper (I) iodide (0.076 g, 0.40 mmol), and 3-bromo-5-methylphenol (1.80 g, 9.60 mmol) were weighed into a large microwave vial. This was then purged with argon then trans-N,N-dimethylcyclohexane-1,2-diamine (0.25 mL, 1.60 mmol) added. To this mixture was then added degassed toluene (8 mL). The mixture was then purged with argon again, the vial sealed, and heated for 1 h at 140° C. in the microwave, then a further 4 h at 135° C. The mixture was cooled, diluted with ethyl acetate and passed through a pad of celite/silica, washing with more ethyl acetate. The dark solution was concentrated in vacuo. The residue was purified by FCC, using 0-40% DCM in EtOAc, to give the title compound (966 mg, 49%). 1H NMR (300 MHz, CDCl3): 1.32 (9H, s), 2.24 (3H, s), 3.82 (2H, br s), 5.49 (1H, s), 6.45-6.52 (1H, m), 6.65-6.71 (1H, m), 6.85-6.91 (1H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440974B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-edfc02741a3e4efc8d0edf36bb885728
출처 메모uspto-grants-2016_09