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HRID 715522作成日:2026年10月25日
6-Ethoxypyridin-3-amine → 1-{[(1S,3S)-3-({[6-(ethyloxy)-3-pyridinyl]amino}methyl)-3-hydroxy-1-methylcyclohexaneyl]methyl}-1H-benzimidazole-6-carbonitrile
https://huagongshe.com/reaction/715522
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 6-Ethoxypyridin-3-amine | HCID 3040301 | — |
| 反応物 | HCID 86716577 | HCID 86716577 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 1-{[(1S,3S)-3-({[6-(ethyloxy)-3-pyridinyl]amino}methyl)-3-hydroxy-1-methylcyclohexaneyl]methyl}-1H-benzimidazole-6-carbonitrile | HCID 71227607 | — |
反応手順
A 5 mL microwave vial was charged with 1-{[(3S,5S)-5-methyl-1-oxaspiro[2.5]oct-5-yl]methyl}-1H-benzimidazole-6-carbonitrile (150 mg, 0.533 mmol),6-(ethyloxy)-3-pyridinamine (221 mg, 1.599 mmol) and MeOH (4 mL). The reaction mixture was stirred and heated to 120° C. for 24 h. The reaction mixture was concentrated down to afford an oil. The oil was purified by silica gel (40 g) loading and initially elluting in DCM through to 6% MeOH/DCM over 18 column volumes to afford 1-{[(1S,3S)-3-({[6-(ethyloxy)-3-pyridinyl]amino}methyl)-3-hydroxy-1-methylcyclohexaneyl]methyl}-1H-benzimidazole-6-carbonitrile as an colorless oil. MS (m/z) 420 (M+H+).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09187464B2 |
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| 出典データセット | uspto-grants-2015_11 |
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| ORD ID | ord-64e313a5748544dc88f11002eac950c6 |
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| 出典メモ | uspto-grants-2015_11 |
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