戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 60676作成日:2026年10月25日

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/reaction/60676

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物trans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
反応物HCID 117729333HCID 117729333—
反応物HCID 178441179HCID 178441179—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒WaterHCID 962—
溶媒O-XyleneHCID 7237—
溶媒Ethyl AcetateHCID 8857—
溶媒Ammonium HydroxideHCID 14923—
生成物{5-Amino-3-tert-butyl-1'-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-1'H-[1,4']bipyrazolyl-3'-yl}-methanolHCID 11772948963%

反応条件

温度150 °C

反応手順

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+].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09440974B2
出典データセットuspto-grants-2016_09
ORD IDord-f5b6f790c30f4ddf9b1104b6c9aeffe1
出典メモuspto-grants-2016_09