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HRID 1517983作成日:2026年10月26日
Sodium Hydroxide → N-Methyl-N-((3R,4R)-4-methyl-1-(phenylmethyl)-3-piperidinyl)-7H-pyrrolo(2,3-d)pyrimidin-4-amine
https://huagongshe.com/reaction/1517983
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | N-(1-Benzyl-4-methylpiperidin-3-yl)-N-methyl-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine | HCID 67010145 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | N-Methyl-N-((3R,4R)-4-methyl-1-(phenylmethyl)-3-piperidinyl)-7H-pyrrolo(2,3-d)pyrimidin-4-amine | HCID 49856703 | 123.2% |
反応手順
To a clean, nitrogen-purged reactor were charged 50% sodium hydroxide solution (210 ml) and (1-benzyl-4-methyl-piperidin-3-yl)-methyl-[7-(toluene-4-sulfonyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-amine (30.0 g, 0.061 mol). The mixture was heated to 95-105° C. for a minimum of 5 hours then cooled to 70-90° C. and water (300 ml) was added. The slurry was cooled to room temperature over a minimum of 1.5 hours and held at room temperature for 1 hour. The solids were isolated by filtration and washed with water (120.0 ml) to obtain 25.2 g of the title compound, water wet.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08232394B2 |
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| 出典データセット | uspto-grants-2012_07 |
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| ORD ID | ord-aea9ea3bc0f34bfd915be602da8fbc4c |
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| 出典メモ | uspto-grants-2012_07 |
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