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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 502457생성일: 2026년 10월 26일

Diisopropylethylamine → Rac-n-[1-(4-chloro-3,5-diethoxy-benzyl)-piperidin-4-yl]-3-(2,3-dihydroxy-propoxy)-5-methoxy-benzamide

https://huagongshe.com/reaction/502457

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참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물1,4-Dioxane hydrochlorideHCID 20443148—
반응물N-[1-(4-Chloro-3,5-diethoxy-benzyl)-piperidin-4-yl]-3-hydroxymethyl-5-methoxy-benzamide 4-Chloro-3,5-diethoxy-benzoic acid ethyl esterHCID 68456709—
반응물rac-3-(2,3-dihydroxy-propoxy)-5-methoxy-N-piperidin-4-yl-benzamide hydrochlorideHCID 68459504—
반응물HCID 131728279HCID 131728279—
용매Acetic AcidHCID 176—
용매EthanolHCID 702—
생성물Rac-n-[1-(4-chloro-3,5-diethoxy-benzyl)-piperidin-4-yl]-3-(2,3-dihydroxy-propoxy)-5-methoxy-benzamideHCID 68455978—

반응 단계

In analogy to the procedure described in example 50k), rac-3-(2,3-dihydroxy-propoxy)-5-methoxy-N-piperidin-4-yl-benzamide hydrochloride (prepared from rac-4-[3-(2,2-dimethyl-[dioxolan-4-ylmethoxy)-5-methoxy-benzoylamino]-piperidine-1-carboxylic acid tert-butyl ester (example 175a) by reaction with HCl/dioxane in EtOH in analogy to the procedure described in example 250b)] was reacted with 4-chloro-3,5-diethoxy-benzaldehyde (example 219), sodium cyanoborohydride, N-ethyl-diisopropylamine and acetic acid in ethanol at 50° C. to yield the title compound as light brown solid. MS: 537.4 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07772253B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-1805e5d9ccf44c06b1a8d948d3ae816d
출처 메모uspto-grants-2010_08