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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 571086생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/571086

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물2-MethylpentaneHCID 7892—
반응물Potassium CarbonateHCID 11430—
반응물4-Iodo-1,2-dimethoxybenzeneHCID 230307—
반응물trans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
반응물HCID 178441179HCID 178441179—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매TolueneHCID 1140—
용매Diethyl EtherHCID 3283—
생성물3-tert-Butyl-1-(3,4-dimethoxyphenyl)-1H-pyrazol-5-amineHCID 71253240—

반응 단계

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+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09024041B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-d00e67e6c0064cadbaed9e1c1d69663e
출처 메모uspto-grants-2015_05