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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 431402생성일: 2026년 10월 25일

Triethylamine → (2,5-dimethyl-4-nitro-2H-pyrazol-3-yl)(3-imidazol-1-yl-propyl)amine

https://huagongshe.com/reaction/431402

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1H-Imidazole-1-propanamineHCID 78736—
반응물5-Chloro-1,3-dimethyl-4-nitro-1H-pyrazoleHCID 279515—
용매DimethylformamideHCID 6228—
생성물(2,5-dimethyl-4-nitro-2H-pyrazol-3-yl)(3-imidazol-1-yl-propyl)amineHCID 1876094356.7%

반응 조건

온도105 °C

반응 단계

0.88 g of 5-chloro-1,3-dimethyl-4-nitro-1H-pyrazole (Aldrich), 1 molar equivalent of triethylamine, 1.1 molar equivalents of 3-imidazol-1-ylpropylamine and 5 ml of N,N-dimethylformamide were introduced into a 25 ml three-necked round-bottomed flask equipped with a magnetic stirrer, a thermometer and a condenser. The reaction medium was maintained at a temperature of about 105° C. for 6 hours. The solvent was evaporated off under vacuum. A black liquid was obtained, which was purified by chromatography on silica gel (ethyl acetate/methanol=4/1). 0.75 g of (2,5-dimethyl-4-nitro-2H-pyrazol-3-yl)(3-imidazol-1-yl-propyl)amine was obtained in the form of white crystals in a yield of 56.7%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06660046B1
출처 데이터셋uspto-grants-2003_12
ORD IDord-1b0976bebc2c494899ef9c1d73b51824
출처 메모uspto-grants-2003_12