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HRID 459076作成日:2026年10月25日

Sodium Iodide → (2S)-2-Methoxy-3-{4-[3-(3-phenyl-benzofuran-6-yloxy)-prop-1-ynyl]-phenyl}-propionic acid

https://huagongshe.com/reaction/459076

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物3-Phenyl-benzofuran-6-olHCID 12273525—
反応物(2S)-3-[4-(3-Chloro-prop-1-ynyl)-phenyl]-2-methoxy-propionic acid ethyl esterHCID 58822943—
溶媒DimethylformamideHCID 6228—
生成物(2S)-2-Methoxy-3-{4-[3-(3-phenyl-benzofuran-6-yloxy)-prop-1-ynyl]-phenyl}-propionic acidHCID 58822838—

反応手順

A solution of (2S)-3-[4-(3-Chloro-prop-1-ynyl)-phenyl]-2-methoxy-propionic acid ethyl ester from Step A (0.071 mmol, 1 eq) in 0.7 ml of DMF in a 16×100 mm tube treated with 3-phenyl-6-hydroxybenzofurane (0.078 mmol, 1.1 eq) Cesium Carbonate (0.213 mmol 3 eq) and NaI (0.071 mmol, 1 eq) and stirred at room temperature overnight. The reactants were filtered and washed with DMF several times. The solvent was evaporated under vacuo and the residue reconstituted in a mixture of Ethanol (2 ml) and NaOH (1M) (1 ml) and stirred at room temperature until reaction is completed by HPLC-MS. Then HCl (1M) was added (until pH=3) and the solvent were eliminated under vacuo. The residue was reconstituted in CH2Cl2/H2O and filtered through a hidrofobic syringer. The organic layer was separated, concentrated and purified by HPLC-MS to get the title compound. MS(ES) for C27H22O5 [M+H]+: 427.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07192982B2
出典データセットuspto-grants-2007_03
ORD IDord-da13f274d6c3495a92c57a5ab0b9f326
出典メモuspto-grants-2007_03