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HRID 571086作成日:2026年10月25日

Nitrogen → 3-tert-Butyl-1-(3,4-dimethoxyphenyl)-1H-pyrazol-5-amine

https://huagongshe.com/reaction/571086

反応式

関与物質

役割名称HCID仕込み量
反応物NitrogenHCID 947—
反応物2-MethylpentaneHCID 7892—
反応物Potassium CarbonateHCID 11430—
反応物4-Iodo-1,2-dimethoxybenzeneHCID 230307—
反応物trans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
反応物HCID 178441179HCID 178441179—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒TolueneHCID 1140—
溶媒Diethyl EtherHCID 3283—
生成物3-tert-Butyl-1-(3,4-dimethoxyphenyl)-1H-pyrazol-5-amineHCID 71253240—

反応手順

To a solution of 4-iodo-1,2-dimethoxybenzene (1.10 g, 4.17 mmol) in anhydrous toluene (5.0 mL) was added 3-tert-butyl-1H-pyrazol-5-amine (638 mg, 4.58 mmol) followed by (1R,2R)—N1,N2-dimethylcyclohexane-1,2-diamine (130 μL, 0.83 mmol) and potassium carbonate (1.15 g, 8.3 mmol). The mixture was purged with N2, copper(I) iodide (40 mg, 0.21 mmol) was added and the reaction mixture was heated at reflux under N2 for 16 hr. The resulting mixture was cooled to RT and was partitioned between EtOAc (100 mL) and water (150 mL). The organic layer was separated and was washed with aq. citric acid solution (10% w/v, 50 mL) followed by brine (50 mL) and then dried and evaporated in vacuo. The residue was purified by flash column chromatography (SiO2, 80 g, EtOAc in isohexane, 0-70%, gradient elution). The impure product so obtained was dissolved in ether (1.0 mL), isohexane (10 mL) was added and the resulting precipitate was collected by filtration to afford the title compound, Intermediate A19, as a purple solid (364 mg, 31%); Rt 3.55 min (Method 1); m/z 276 (M+H)+ (ES+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09024041B2
出典データセットuspto-grants-2015_05
ORD IDord-d00e67e6c0064cadbaed9e1c1d69663e
出典メモuspto-grants-2015_05