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HRID 2182843作成日:2026年10月27日

Lansoprazole → (4-{2-[3-Methyl-4-(2,2,2-trifluoro-ethoxy)-pyridin-2-ylmethanesulfinyl]-benzimidazole-1-sulfonyl}phenoxy)acetic Acid 2-(toluene-4-sulfonyl)ethyl Ester

https://huagongshe.com/reaction/2182843

反応式

関与物質

役割名称HCID仕込み量
反応物LansoprazoleHCID 3883—
反応物Sodium hydrideHCID 24758—
反応物Sodium BicarbonateHCID 516892—
反応物SulfurochloridateHCID 21989438—
反応物Acetic acid 2-(toluene-4-sulfonyl)ethyl esterHCID 58426230—
反応物2-Tosylethyl 2-(4-(chlorosulfonyl)phenoxy)acetateHCID 59316688—
溶媒DichloromethaneHCID 6344—
生成物(4-{2-[3-Methyl-4-(2,2,2-trifluoro-ethoxy)-pyridin-2-ylmethanesulfinyl]-benzimidazole-1-sulfonyl}phenoxy)acetic Acid 2-(toluene-4-sulfonyl)ethyl EsterHCID 2078642394%

反応手順

To a heterogeneous solution of 2-[3-methyl-4-(2,2,2-trifluoroethoxy)pyridin-2-ylmethanesulfinyl]-1H-benzimidazole (900 mg, 2.44 mmol) in 30 mL of CH2Cl2 was added 70 mg of NaH (2.92 mmol) at room temperature, during which time the mixture became homogeneous. To this clear reaction mixture was added the 4-chlorosulfonylphenoxy)acetic acid 2-(toluene-4-sulfonyl)ethyl ester (Intermediate 4, 1.26 g, 2.92 mmol, 1.2 eq). About 1 g of solid NaHCO3 was added after the chlorosulfonate has dissolved completely in the reaction mixture. (Without addition of NaHCO3 the mixture became black when the reaction was complete.) Thereafter the solvent was removed by evaporation and the residual oil was purified by column chromatography (silica gel, CH2Cl2 to 4% MeOH in CH2Cl2) to give 1.75 g (94%) of the desired product (Intermediate 5) as an off-white foam.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06897227B2
出典データセットuspto-grants-2005_05
ORD IDord-fedb963048944885a00ed1ff4b580582
出典メモuspto-grants-2005_05