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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1053551생성일: 2026년 10월 27일

Trimethylamine → 3-{2-[2-hydroxy-1-(3-hydroxyoctyl)-2,3,3a,4,9,9a-hexahydro-1H-cyclopenta[b]naphthalen-5-yloxy]acetoxy}propionic acid

https://huagongshe.com/reaction/1053551

반응식

참여 물질

역할이름HCID투입량
반응물TrimethylamineHCID 1146—
반응물Propanoic acid, 3-hydroxy-, phenylmethyl esterHCID 84459—
반응물Bis(2-oxo-3-oxazolidinyl)phosphinic chlorideHCID 152842—
반응물{2-hydroxy-1-[3-(tetrahydropyran-2-yloxy)octyl]-2,3,3a,4,9,9a-hexahydro-1H-cyclopenta[b]naphthalen-5-yloxy}acetic acidHCID 90281645—
용매DichloromethaneHCID 6344—
용매tert-Butyl methyl etherHCID 15413—
생성물3-{2-[2-hydroxy-1-(3-hydroxyoctyl)-2,3,3a,4,9,9a-hexahydro-1H-cyclopenta[b]naphthalen-5-yloxy]acetoxy}propionic acidHCID 121480745—

반응 단계

To a solution of Compound B (120 mg, 0.25 mmol), benzyl 3-hydroxypropionate (54 mg, 0.30 mmol) and trimethylamine (140 μL, 1.0 mmol) in DCM (4 mL) was added BOP—Cl (95 mg, 0.38 mmol). The reaction mixture was stirred at RT for 16 hr under nitrogen, diluted with MTBE, washed with brine, dried over sodium sulfate, and concentrated to an oil that was purified by silica gel chromatography. A solution of the THP-protected diester in ethanol (4 mL) was treated with PPTS (50 mg), stirred at 50° C. for 4 hr, and concentrated to an oil that was purified by silica gel chromatography. A solution of the THP-deprotected diester in dioxane (5 mL) was treated with wet 5% Pd/C (20 mg) and stirred for 24 hr under a balloon of hydrogen. The reaction mixture was filtered and concentrated to give crude Compound II-4. MS: m/z 485 [M+Na]+

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09394227B1
출처 데이터셋uspto-grants-2016_07
ORD IDord-99aa46029a874eeaa0d37620c04c9656
출처 메모uspto-grants-2016_07