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HRID 460359作成日:2026年10月24日

Acetic Acid → 3-[7-Ethoxy-3-(3-fluoro-phenylamino)-2,4-dihydro-indeno[1,2-c]pyrazol-6-yloxy]-propan-1-ol

https://huagongshe.com/ja/reaction/460359

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物HydrazineHCID 9321—
反応物3-Fluorophenyl isothiocyanateHCID 9834—
反応物6-Ethoxy-5-[3-(tetrahydro-pyran-2-yloxy)-propoxy]-indan-1-oneHCID 18445806—
反応物Lithium hexamethyldisilaneHCID 57425481—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物3-[7-Ethoxy-3-(3-fluoro-phenylamino)-2,4-dihydro-indeno[1,2-c]pyrazol-6-yloxy]-propan-1-olHCID 178465802—

反応手順

To a mixture of 6-Ethoxy-5-[3-(tetrahydro-pyran-2-yloxy)-propoxy]-indan-1-one (Intermediate AA) (0.100 g, 0.0003 mol), 3-fluorophenyl isothiocyanate (Compound 4a) (0.043 mL, 0.00036 mol) and THF (3 mL) was added lithium hexamethyldisilane (0.360 mL, 0.00036 mol) dropwise at room temperature with stirring. The reaction mixture was stirred for 48 h. Hydrazine (0.011 mL, 0.00036 mol) and acetic acid (0.021 mL, 0.00036 mol) was added to the reaction mixture, which was then heated at reflux temperature for 12 h. The reaction solution was then diluted with ethyl acetate, washed with water and dried over MgSO4. The solvent was removed in vacuo and the crude material was purified on the reverse phase HPLC and converted to the desired product upon standing in the 0.1% TFA solution. Lyophilization yielded the title compound as a white powder. MS m/z 384.2 (M+H)+;

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07196110B2
出典データセットuspto-grants-2007_03
ORD IDord-fc8a575e0cc74445b882d49375af1e7d
出典メモuspto-grants-2007_03