참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tesmilifene Hydrochloride | HCID 175534 | — |
| 반응물 | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| 반응물 | 5-Bromo-2-nitrothiophene-3-carbaldehyde oxime | HCID 72315997 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 5-Bromo-2-nitrothiophene-3-carboxamide | HCID 53402948 | — |
반응 단계
5-Bromo-2-nitrothiophene-3-carbaldehyde oxime (45 g, 179 mmol), p-toluenesulfonic acid monohydrate (2.73 g, 14.34 mmol), dppe (1.428 g, 3.58 mmol) and Ru(PPh3)3(CO)H2 (3.29 g, 3.58 mmol) were taken up in toluene (750 mL). The flask was evacuated and back-filled with N2 (3×) before stirring at 111° C. under N2 for 24 hours. After cooling to room temperature, the reaction mixture was purified directly by flash silica gel column chromatography (0-100% EtOAc-toluene) to give the title compound as brown needles after recrystallising from EtOH-hexanes.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08367706B2 |
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| 출처 데이터셋 | uspto-grants-2013_02 |
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| ORD ID | ord-4af59e4c2c164cb9bd58bc3d50117f2d |
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| 출처 메모 | uspto-grants-2013_02 |
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