참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Bromine | HCID 24408 | — |
| 반응물 | 4-Amino-2,6-dimethylpyridine | HCID 77047 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 생성물 | 3-Bromo-2,6-dimethyl-4-pyridinamine | HCID 10512262 | 40% |
반응 단계
A solution of 2,6-dimethylpyridin-4-ylamine (2.00 g, 16.4 mmol) in 5 mL of acetic acid was treated dropwise with a solution of bromine (0.84 mL, 16.3 mmol) in 2 mL of acetic acid at room temperature in a water bath over a period of 10 minutes. After I hour, the resulting slurry was treated with 40 mL of 20% sodium hydroxide solution and extracted with three 100 mL portions of dichloromethane (CH2Cl2). The combined extracts were dried over magnesium sulfate, filtered, and concentrated in vacuo. The resulting solid (starting material-desired product-dibromo byproduct (1:3:1)) was dissolved in 100 mL of hot hexanes and hot filtered to remove the insoluble starting material. The filtrate was allowed to cool to room temperature, which gave the title product as fine white needles (1.30 g, 40% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08741897B2 |
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| 출처 데이터셋 | uspto-grants-2014_06 |
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| ORD ID | ord-db834648189a4724bd11503d9cc4ca6c |
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| 출처 메모 | uspto-grants-2014_06 |
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