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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

反応式

関与物質

役割名称HCID仕込み量
反応物6-Ethoxypyridin-3-amineHCID 3040301—
反応物HCID 86716577HCID 86716577—
溶媒MethanolHCID 887—
生成物1-{[(1S,3S)-3-({[6-(ethyloxy)-3-pyridinyl]amino}methyl)-3-hydroxy-1-methylcyclohexaneyl]methyl}-1H-benzimidazole-6-carbonitrileHCID 71227607—

反応条件

温度120 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US09187464B2
出典データセットuspto-grants-2015_11
ORD IDord-64e313a5748544dc88f11002eac950c6
出典メモuspto-grants-2015_11