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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1692416생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1692416

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참여 물질

역할이름HCID투입량
반응물(4-Bromo-2,6-dimethyl-phenyl)-[4-((S)-2-hydroxymethyl-pyrrolidin-1-yl)-piperidin-1-yl]-methanoneHCID 44473778—
반응물4,6-Dimethyl-2-(3-trifluoromethyl-phenyl)-pyrimidine-5-carboxylic acidHCID 62744716—
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[4,6-Dimethyl-2-(3-trifluoromethyl-phenyl)-pyrimidin-5-yl]-(4-hydroxy-[1,4']bipiperidinyl-1'-yl)-methanoneHCID 57580525—

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In analogy to the procedures described for intermediate 1 and for intermediate 4 B, 4,6-dimethyl-2-(3-trifluoromethyl-phenyl)-pyrimidine-5-carboxylic acid (intermediate 5) 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: 463.3 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08153805B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-5d265573b39e475b87d4da89aebff45c
출처 메모uspto-grants-2012_04