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HRID 271080作成日:2026年10月25日
Ethyl 4,6-dichloropyridazine-3-carboxylate → (4,6-Dichloro-pyridazin-3-yl)-(2-methoxy-phenyl)-methanone
https://huagongshe.com/reaction/271080
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethyl 4,6-dichloropyridazine-3-carboxylate | HCID 53428795 | — |
| 反応物 | HCID 178489560 | HCID 178489560 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (4,6-Dichloro-pyridazin-3-yl)-(2-methoxy-phenyl)-methanone | HCID 59834303 | 78.2% |
反応手順
4,6-Dichloro-pyridazine-3-carboxylic acid ethyl ester (1.032 g, 4.67 mmol, prepared as described by Xie et al., WO 2004031174) was dissolved in 25 ml dry THF, and the reaction mixture was cooled in a dry ice/acetone bath for 15 minutes. 2-Methoxyphenyl magnesium bromide (7 mL of 1M solution in THF, 7.00 mmol) was added, and the reaction mixture was stirred for 8 hours under nitrogen at −78° C. Silica gel (11.0 g) was added, and the reaction mixture was allowed to warm to room temperature. Solvent was removed under reduced pressure, and the residue was purified by flash chromatography (0% to 20% EtOAc/Hexanes) to yield 1.029 g (3.65 mmol, 78%) of (4,6-dichloro-pyridazin-3-yl)-(2-methoxy-phenyl)-methanone as a yellow solid. Mass Spec. M+H=283.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07452880B2 |
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| 出典データセット | uspto-grants-2008_11 |
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| ORD ID | ord-253eb133e26945d5a80a0781a1b56b86 |
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| 出典メモ | uspto-grants-2008_11 |
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