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HRID 1738632作成日:2026年10月25日

5-Isopropylpyridine-2-sulfonyl chloride → Methyl 4-(2-chloro-5-methoxy-phenoxy)-3-(5-isopropyl-pyridine-2-sulphonylamino)-5-[2-(tetrahydro-pyran-2-yloxy)-ethoxy]-benzoate

https://huagongshe.com/reaction/1738632

反応式

関与物質

役割名称HCID仕込み量
反応物5-Isopropylpyridine-2-sulfonyl chlorideHCID 22281918—
反応物Methyl 3-amino-4-(2-chloro-5-methoxy-phenoxy)-5-[2-(tetrahydro-pyran-2-yloxy)-ethoxy]-benzoateHCID 23288632—
溶媒TolueneHCID 1140—
溶媒Pyridine tolueneHCID 22007288—
生成物Methyl 4-(2-chloro-5-methoxy-phenoxy)-3-(5-isopropyl-pyridine-2-sulphonylamino)-5-[2-(tetrahydro-pyran-2-yloxy)-ethoxy]-benzoateHCID 23288580—

反応手順

1.12 g of methyl 3-amino-4-(2-chloro-5-methoxy-phenoxy)-5-[2-(tetrahydro-pyran-2-yloxy)-ethoxy]-benzoate were dissolved in a mixture of toluene/pyridine (20 ml/30 ml) treated dropwise while cooling with ice with a solution of 1.05 g of 5-isopropylpyridine-2-sulphonyl chloride in toluene (30 ml) and subsequently stirred at room temperature for 24 hours. The reaction mixture was poured on to ice/3M HCl, the product was extracted with ethyl acetate and the organic phase was washed with water and dried over magnesium sulphate. After removing the solvent there was obtained the desired methyl 4-(2-chloro-5-methoxy-phenoxy)-3-(5-isopropyl-pyridine-2-sulphonylamino)-5-[2-(tetrahydro-pyran-2-yloxy)-ethoxy]-benzoate as a yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05962682
出典データセットuspto-grants-1999_10
ORD IDord-9b5a3f47561043edadb8fe1b21cc140b
出典メモuspto-grants-1999_10