참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Nitric Acid | HCID 944 | — |
| 반응물 | Ammonium Hydroxide | HCID 14923 | — |
| 반응물 | 2-Amino-5-chloro-4-methylpyridine | HCID 318186 | — |
| 용매 | Sulfuric Acid | HCID 1118 | — |
| 생성물 | 5-Chloro-4-methyl-3-nitropyridin-2-amine | HCID 21464136 | 58.6% |
반응 단계
5-chloro-4-methylpyridin-2-amine (30 g, 210 mmol) was dissolved in concentrated sulfuric acid (150 mL), and the solution was cooled to −10° C. Nitric acid (36 mL, 806 mmol) was added dropwise. The reaction mixture was stirred at 55° C. for 3 hours. The reaction mixture was poured into an ice/water mixture, and the pH was adjusted to 8 by addition of concentrated aqueous ammonium hydroxide (22%). The resulting suspension was filtered, and the solids were washed with water and dried under vacuum to provide the title compound (23 g, 123 mmol, 58.3% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09321764B2 |
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| 출처 데이터셋 | uspto-grants-2016_04 |
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| ORD ID | ord-a2100a516536452dab4483736fdd0f16 |
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| 출처 메모 | uspto-grants-2016_04 |
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