참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 1H-Imidazole-1-propanamine | HCID 78736 | — |
| 반응물 | 5-Chloro-1,3-dimethyl-4-nitro-1H-pyrazole | HCID 279515 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (2,5-dimethyl-4-nitro-2H-pyrazol-3-yl)(3-imidazol-1-yl-propyl)amine | HCID 18760943 | 56.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06660046B1 |
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| 출처 데이터셋 | uspto-grants-2003_12 |
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| ORD ID | ord-1b0976bebc2c494899ef9c1d73b51824 |
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| 출처 메모 | uspto-grants-2003_12 |
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