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HRID 1046528作成日:2026年10月27日
4-(Methanesulfonylmethyl)cyclohexan-1-amine → 2-{3-[2-(4-Methanesulfonylmethyl-cyclohexylamino)-pyrimidin-4-yl]-imidazo[1,2-a]pyridin-8-yl}-propan-2-ol
https://huagongshe.com/reaction/1046528
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 4-(Methanesulfonylmethyl)cyclohexan-1-amine | HCID 58345904 | — |
| 反応物 | 2-[3-(2-Methylsulfinyl-pyrimidin-4-yl)-imidazo[1,2-a]pyridin-8-yl]-propan-2-ol | HCID 66616285 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 生成物 | 2-{3-[2-(4-Methanesulfonylmethyl-cyclohexylamino)-pyrimidin-4-yl]-imidazo[1,2-a]pyridin-8-yl}-propan-2-ol | HCID 58553169 | 52.8% |
反応手順
A mixture of 2-[3-(2-methylsulfinyl-pyrimidin-4-yl)-imidazo[1,2-a]pyridin-8-yl]-propan-2-ol (75 mg), 4-methanesulfonylmethyl-cyclohexylamine (162 mg), and TEA (0.165 mL) in NMP (2 mL) was stirred at 100° C. overnight. The reaction mixture was then cooled to RT, and diluted with water. The resulting precipitate was filtered and dried, then purified by ISCO using 100% DCM to 10% MeOH/DCM. The fractions were collected, concentrated, and titurated with EtOAc. The resulting solid was filtered and dried at 50° C. under vacuum overnight to provide 2-{3-[2-(4-methanesulfonylmethyl-cyclohexylamino)-pyrimidin-4-yl]-imidazo[1,2-a]pyridin-8-yl}-propan-2-ol (Compound 1, 55.5 mg). Mp=223-224° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08569306B2 |
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| 出典データセット | uspto-grants-2013_10 |
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| ORD ID | ord-8172da2e90f4453281532ffa792a72a2 |
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| 出典メモ | uspto-grants-2013_10 |
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