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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2182843생성일: 2026년 10월 26일

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

반응식

참여 물질

역할이름HCID투입량
반응물LansoprazoleHCID 3883—
반응물Sodium hydrideHCID 24758—
반응물Sodium BicarbonateHCID 516892—
반응물SulfurochloridateHCID 21989438—
반응물HCID 58426230HCID 58426230—
반응물HCID 59316688HCID 59316688—
용매DichloromethaneHCID 6344—
생성물(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%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06897227B2
출처 데이터셋uspto-grants-2005_05
ORD IDord-fedb963048944885a00ed1ff4b580582
출처 메모uspto-grants-2005_05