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HRID 74864作成日:2026年10月26日
1,2-Epoxy-3-methoxypropane → (S)-3-((2-(5-chloro-1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-5-fluoropyrimidin-4-ylamino)piperidin-1-yl)-3-methoxypropan-2-ol
https://huagongshe.com/reaction/74864
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 1,2-Epoxy-3-methoxypropane | HCID 13589 | — |
| 反応物 | 2-[5-chloro-1-(p-tolylsulfonyl)pyrrolo[2,3-b]pyridin-3-yl]-5-fluoro-N-[(3S)-3-piperidyl]pyrimidin-4-amine | HCID 67285119 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | (S)-3-((2-(5-chloro-1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-5-fluoropyrimidin-4-ylamino)piperidin-1-yl)-3-methoxypropan-2-ol | HCID 86762718 | — |
反応手順
To a solution of 2-[5-chloro-1-(p-tolylsulfonyl)pyrrolo[5,4-b]pyridin-3-yl]-5-fluoro-N-[(3S)-3-piperidyl]pyrimidin-4-amine, 1c, (0.20 g, 0.40 mmol) in ethanol was added 2-(methoxymethyl)oxirane (0.04 mL, 0.40 mmol). The reaction mixture was heated in a microwave reactor at 140° C. for 5 minutes. The reaction was evaporated to dryness and the resulting residue was purified via silica gel chromatography (0-10% MeOH: CH2Cl2) to afford the desired product (1d).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08829007B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-36f9b358ed36485fb98f406c9949dab4 |
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| 出典メモ | uspto-grants-2014_09 |
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