戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1645651作成日:2026年10月25日

3,3-Dimethyl-1,5-dioxaspiro[5.5]undecan-9-ol → 2-(((4-((3,3-Dimethyl-1,5-dioxaspiro[5.5]undec-9-yl)oxy)-3-methylpyridin-2-yl)methyl)sulfinyl)-1h-benzimidazole sodium salt

https://huagongshe.com/reaction/1645651

反応式

関与物質

役割名称HCID仕込み量
反応物3,3-Dimethyl-1,5-dioxaspiro[5.5]undecan-9-olHCID 12470096—
反応物2-(((4-(((4r)-2,2-Dimethyl-1,3-dioxolan-4-yl)methoxy)-3-methylpyridin-2-yl)methyl)sulfinyl)-1h-benzimidazole sodium saltHCID 66776552—
生成物2-(((4-((3,3-Dimethyl-1,5-dioxaspiro[5.5]undec-9-yl)oxy)-3-methylpyridin-2-yl)methyl)sulfinyl)-1h-benzimidazole sodium saltHCID 66776456—

反応手順

The same procedure as in the steps (14a) to (14e) of Example 14 was repeated using the 3,3-dimethyl-1,5-dioxaspiro[5.5]undecan-9-ol obtained in the step (81a) above to obtain the title compound (275 mg, the total yield of 5 steps: 3.3%) as a white solid. Note that in the same process as in the step (14b), after acetic anhydride was added, 10 equivalents of triethylamine relative to pyridine 1-oxide derivative was added to perform the reaction. In the same process as in the step (14c), tetrahydrofuran was used as a solvent instead of ethanol.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08124780B2
出典データセットuspto-grants-2012_02
ORD IDord-dcf231f787234b3898012c1cb010ce88
出典メモuspto-grants-2012_02