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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 411620생성일: 2026년 10월 26일

Omeprazole → 1-[(benzotriazol-1-yl)methyl]-6-methoxy-2-[[(3,5-dimethyl-4-methoxy-2-pyridyl)methyl]sulfinyl]-1H-benzimidazole

https://huagongshe.com/reaction/411620

반응식

참여 물질

역할이름HCID투입량
반응물OmeprazoleHCID 4594—
반응물1-(Chloromethyl)-1H-benzotriazoleHCID 3328222—
반응물1-[(benzotriazol-1-yl)methyl]-5-methoxy-2-[[(3,5-dimethyl-4-methoxy-2-pyridyl)methyl]sulfinyl]-1H-benzimidazoleHCID 18541198—
반응물Sodium t-butoxideHCID 23676156—
용매DichloromethaneHCID 6344—
용매Chloroform methanolHCID 21584188—
생성물1-[(benzotriazol-1-yl)methyl]-6-methoxy-2-[[(3,5-dimethyl-4-methoxy-2-pyridyl)methyl]sulfinyl]-1H-benzimidazoleHCID 18541128—

반응 조건

온도30 °C

반응 단계

5-Methoxy-2-[[(3,5-dimethyl-4-methoxy-2-pyridyl)methyl]sulfinyl]-1H-benzimidazole (172 mg) was dissolved in 20 ml of dichloromethane. Sodium tert-butoxide (55 mg) and 1-(chloromethyl)-1H-benzotriazole (85 mg) was added. The reaction mixture was stirred at 30° C. for 3 days. TLC analysis (developing solvent; chloroform-methanol 15:1) showed major one spot of 1-[(benzotriazol-1-yl)methyl]-5-methoxy-2-[[(3,5-dimethyl-4-methoxy-2-pyridyl)methyl]sulfinyl]-1H-benzimidazole above 5-methoxy-2-[[(3,5-dimethyl-4-methoxy-2-pyridyl)methyl]sulfinyl]-1H-benzimidazole. The titled product was purified by preparative thin layer chromatography. 195 mg of product, a mixture of 1-[(benzotriazol-1-yl)methyl]-5-methoxy-2-[[(3,5-dimethyl-4-methoxy-2-pyridyl)methyl]sulfinyl]-1H-benzimidazole and 1-[(benzotriazol-1-yl)methyl]-6-methoxy-2-[[(3,5-dimethyl-4-methoxy-2-pyridyl)methyl]sulfinyl]-1H-benzimidazole was obtained (3:2 ratio).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06559167B1
출처 데이터셋uspto-grants-2003_05
ORD IDord-1b68d613025a437985ac12dc9d4fd244
출처 메모uspto-grants-2003_05