참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | 2-Chloro-3-nitropyridine | HCID 79613 | — |
| 반응물 | HCID 178448414 | HCID 178448414 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 7-Chloro-2,3-dimethyl-1H-pyrrolo[2,3-c]pyridine | HCID 11636927 | 30% |
반응 단계
2-Chloro-3-nitropyridine (8 g, 50.46 mmol) was dissolved in anhydrous tetrahydrofuran (200 ml) at nitrogen atmosphere. 1-Methyl-1-propenyl magnesium bromide (0.5M in tetrahydrofuran solution, 252 ml, 126.15 mmol) was slowly added at −78° C. to the solution. The reaction mixture was stirred for 2 hours at −20° C. and 20% ammonium chloride solution was added thereto. The reaction mixture was extracted with ethyl acetate and then concentrated under reduced pressure. The resulting residue was purified with silica gel column chromatography (ethyl acetate/n-hexane=1/3, v/v) to give 2.73 g of the titled compound as a pale yellow solid. (Yield: 30%)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07662832B2 |
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| 출처 데이터셋 | uspto-grants-2010_02 |
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| ORD ID | ord-8defa0b274054bbb9a830e8784657c63 |
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| 출처 메모 | uspto-grants-2010_02 |
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