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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1692417생성일: 2026년 10월 27일

(4-Bromo-2,6-dimethyl-phenyl)-[4-((S)-2-hydroxymethyl-pyrrolidin-1-yl)-piperidin-1-yl]-methanone → [2-(3,5-Bis-trifluoromethyl-phenyl)-4,6-dimethyl-pyrimidin-5-yl]-(4-hydroxy-[1,4']bipiperidinyl-1'-yl)-methanone

https://huagongshe.com/reaction/1692417

반응식

참여 물질

역할이름HCID투입량
반응물(4-Bromo-2,6-dimethyl-phenyl)-[4-((S)-2-hydroxymethyl-pyrrolidin-1-yl)-piperidin-1-yl]-methanoneHCID 44473778—
반응물[2-(3,5-Bis-trifluoromethyl-phenyl)-4,6-dimethyl-pyrimidin-5-yl]-(4-pyrrolidin-1-yl-piperidin-1-yl)-methanoneHCID 57580536—
반응물Benzoic acid [1,4']bipiperidinyl-4-yl esterHCID 66901535—
반응물(4-Bromo-2,6-dimethyl-phenyl)-(4-pyrrolidin-1-yl-piperidin-1-yl)-methanoneHCID 66901599—
생성물[2-(3,5-Bis-trifluoromethyl-phenyl)-4,6-dimethyl-pyrimidin-5-yl]-(4-hydroxy-[1,4']bipiperidinyl-1'-yl)-methanoneHCID 57580557—

반응 단계

In analogy to the procedures described for intermediate 1 and for intermediate 4 B, 2-(3,5-bis-trifluoromethyl-phenyl)-4,6-dimethyl-pyrimidine-5-carboxylic acid (example 15) was converted into its acid chloride, reacted with benzoic acid [1,4′]bipiperidinyl-4-yl ester (example 22) and subsequently saponified to give the title compound as colorless solid. MS: 531.1 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08153805B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-2a98c80825eb4e9e99a6bab6a7e0abfe
출처 메모uspto-grants-2012_04