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HRID 368745作成日:2026年10月26日

4-(Methylthio)benzenesulfonyl chloride → Methyl 4-(2-methoxy-phenoxy)-3-(4-methylsulphanyl-benzenesulphonylamino)-5-[2-(tetrahydro-pyran-2-yloxy)-ethoxy]-benzoate

https://huagongshe.com/reaction/368745

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Methylthio)benzenesulfonyl chlorideHCID 11138731—
反応物Methyl 3-amino-4-(2-methoxy-phenoxy)-5-[2-(tetrahydro-pyran-2-yloxy)-ethoxy]-benzoateHCID 23288571—
溶媒PyridineHCID 1049—
溶媒TolueneHCID 1140—
生成物Methyl 4-(2-methoxy-phenoxy)-3-(4-methylsulphanyl-benzenesulphonylamino)-5-[2-(tetrahydro-pyran-2-yloxy)-ethoxy]-benzoateHCID 23288593—

反応手順

0.626 g of methyl 3-amino-4-(2-methoxy-phenoxy)-5-[2-(tetrahydro-pyran-2-yloxy)-ethoxy]-benzoate was dissolved in pyridine (30 ml), treated dropwise while cooling with ice with a solution of 0.593 g of 4-methylsulphanylbenzenesulphonyl chloride in toluene (10 ml) and subsequently stirred at RT for 20 hours. The reaction mixture was poured on to ice/3M HCl, the product was extracted with ethyl acetate and the organic phase was dried over magnesium sulphate. After removing the solvent there was obtained methyl 4-(2-methoxy-phenoxy)-3-(4-methylsulphanyl-benzenesulphonylamino)-5-[2-(tetrahydro-pyran-2-yloxy)-ethoxy]-benzoate as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06133442
出典データセットuspto-grants-2000_10
ORD IDord-9bcfb87929c74cddb7290bb769124924
出典メモuspto-grants-2000_10