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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 323484생성일: 2026년 10월 24일

1-(3,4,5-Trimethoxybenzoyl)-3-(4-fluorophenyl)-3-(2-methanesulfonyloxyethyl)pyrrolidine → 1-(3,4,5-trimethoxybenzoyl)-3-(2-(4-(1H-benzimidazol-2-yl-amino)piperidin-1-yl)ethyl)-3-(4-fluorophenyl) pyrrolidine

https://huagongshe.com/ko/reaction/323484

반응식

참여 물질

역할이름HCID투입량
반응물1-(3,4,5-Trimethoxybenzoyl)-3-(4-fluorophenyl)-3-(2-methanesulfonyloxyethyl)pyrrolidineHCID 18464932—
반응물(1H-benzimidazol-2-yl)(piperidin-4-yl)amine hydriodic acidHCID 86754231—
용매Ethyl acetate hexaneHCID 21226206—
생성물1-(3,4,5-trimethoxybenzoyl)-3-(2-(4-(1H-benzimidazol-2-yl-amino)piperidin-1-yl)ethyl)-3-(4-fluorophenyl) pyrrolidineHCID 9916763—

반응 단계

Prepare by the method of Example 4.1 using 1-(3,4,5-trimethoxybenzoyl)-3-(4-fluorophenyl)-3-(2-methanesulfonyloxyethyl)pyrrolidine (2.65 g, 5.5 mmol) (prepared from (+)-1-(3,4,5-trimethoxybenzoyl)-3-(4-fluorophenyl)-3-(2-hydroxyethyl)pyrrolidine) and (1H-benzimidazol-2-yl)(piperidin-4-yl)amine hydriodic acid salt (3.9 g, 8.25 mmol) to give, after chromatography on silica gel eluting with methanol/ethyl acetate 1/1, the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06211199B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-5aeeef697d5042eca7b87b22cc6b2516
출처 메모uspto-grants-2001_04