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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 60676생성일: 2026년 10월 24일

Potassium Carbonate → {5-Amino-3-tert-butyl-1'-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-1'H-[1,4']bipyrazolyl-3'-yl}-methanol

https://huagongshe.com/ko/reaction/60676

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참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물trans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
반응물HCID 117729333HCID 117729333—
반응물HCID 178441179HCID 178441179—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매WaterHCID 962—
용매O-XyleneHCID 7237—
용매Ethyl AcetateHCID 8857—
용매Ammonium HydroxideHCID 14923—
생성물{5-Amino-3-tert-butyl-1'-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-1'H-[1,4']bipyrazolyl-3'-yl}-methanolHCID 11772948963%

반응 조건

온도150 °C

반응 단계

A solution of Intermediate 74d (0.51 g, 1.45 mmol) in xylene (2.4 mL) was treated with 3-(tert-butyl)-1H-pyrazol-5-amine (0.18 g, 1.32 mmol) then potassium carbonate (0.38 g, 2.76 mmol), trans-N,N′-Dimethyl-1,2-cyclohexanediamine (0.037 g, 0.26 mmol) and copper (I) iodide (0.013 g, 0.066 mmol) were added. The mixture was degassed then heated at 150° C. for 4 h using microwave irradiation. Another portion of copper (I) iodide (0.006 g, 0.03 mmol) was added and the reaction mixture heated at 150° C. for a further 2 h using microwave irradiation. The mixture was diluted with water (1 mL), conc. aqueous ammonium hydroxide (1 mL) and EtOAc (1 mL) and the phases separated. The aqueous layer was then extracted with EtOAc (2×). The combined organic layers were washed with water and brine, dried (Na2SO4), filtered and evaporated in vacuo. The residue was purified by FCC, using 0-5% MeOH in DCM to give the title compound as a dark green gum (0.30 g, 63%). LCMS (Method 3): Rt 2.46 min, m/z 364 [MH+].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440974B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-f5b6f790c30f4ddf9b1104b6c9aeffe1
출처 메모uspto-grants-2016_09