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HRID 1168532作成日:2026年10月27日
1-Boc-1-methylhydrazine → ethyl 2-(2,3-difluoro-5-iodobenzoyl)-3-[2-methyl-2-[(2-methylpropan-2-yl)oxycarbonyl]hydrazinyl]prop-2-enoate
https://huagongshe.com/reaction/1168532
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 1-Boc-1-methylhydrazine | HCID 3748280 | — |
| 反応物 | Ethyl 2-(2,3-Difluoro-5-iodobenzoyl)-3-ethoxy-2-propenoate | HCID 69879816 | — |
| 溶媒 | tert-Butanol | HCID 6386 | — |
| 生成物 | ethyl 2-(2,3-difluoro-5-iodobenzoyl)-3-[2-methyl-2-[(2-methylpropan-2-yl)oxycarbonyl]hydrazinyl]prop-2-enoate | HCID 178472139 | 92.2% |
反応手順
A solution of ethyl 2-(2,3-difluoro-5-iodobenzoyl)-3-ethoxy-2-propenoate (Preparation 21, 7.80 g) in tert-butanol (40 mL) is cooled with a cold water bath and a solution of tert-butyl 1-methylhydrazinecarboxylate (2.92 g) in tert-butanol (4 mL) is added. The cooling bath is removed, the mixture is stirred for 5 min at ambient temperature, and then is heated in an oil bath at 45° C. for 40 min. The reaction mixture is poured into 100 mL of crushed ice/water and extracted two times with ethyl acetate. The combined organic layers are dried (Na2SO4) and concentrated in vacuo. The crude product is purified by chromatography, using 300 g of silica gel, packed and eluted with EtOAc/heptane (1/3), to afford 8.95 g (92%) of the title compound as a yellow oily foam. Physical characteristics: 1H NMR (CDCl3) δ8.14, 8.07, 7.59-7.49, 7.46-7.41, 4.07, 3.30, 3.26, 1.50, 1.09, 0.97; MS (ESI+) m/z 511 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06624159B2 |
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| 出典データセット | uspto-grants-2003_09 |
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| ORD ID | ord-64a0e742feee401781161d683297aaa4 |
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| 出典メモ | uspto-grants-2003_09 |
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