참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tributyltin Chloride | HCID 15096 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 2-iodo-N-methylisonicotinamide | HCID 57516643 | — |
| 반응물 | HCID 178418918 | HCID 178418918 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-methyl-2-tributylstannanyl-isonicotinamide | HCID 57516644 | 31% |
반응 단계
In a round-bottomed flask, 2-iodo-N-methylisonicotinamide (0.18 g, 0.69 mmol) was dissolved in THF (3.9 mL) and sodium hydride (60% dispersion in mineral oil, 33 mg, 0.83 mmol) was added. The reaction mixture was stirred at room temperature for 10 min then cooled to −16° C. (NaCl/ice bath) and isopropylmagnesium chloride (2.0M solution in THF, 0.39 mL, 0.780 mmol) was added dropwise. The reaction mixture was stirred at −16° C. for 40 min then tributylchlorostannane (0.22 mL, 0.81 mmol) was slowly added. The reaction mixture was allowed to warm to room temperature and stirred for 2 h then quenched with saturated NH4Cl solution and then extracted with 50 mL EtOAc (2×). The combined organic layers were washed with 5 mL water and 5 mL brine then dried over sodium sulfate, filtered and concentrated. The residue was chromatographed over 12 g silica gel with EtOAc/Hexanes (contains 1% Triethylamine) (gradient: 0-30% EtOAc). All fractions containing product were combined and concentrated to afford 89 mg (31%) of N-methyl-2-tributylstannanyl-isonicotinamide as a colorless oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08518945B2 |
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| 출처 데이터셋 | uspto-grants-2013_08 |
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| ORD ID | ord-71fbbfc824cf4b1f8b92ea625199e265 |
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| 출처 메모 | uspto-grants-2013_08 |
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