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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 240374생성일: 2026년 10월 24일

Triethylamine → (4-Benzyl-4-hydroxypiperidin-1-yl)(3-methyl-5-(pyridin-4-yl)-1,2-oxazol-4-yl)methanone

https://huagongshe.com/ko/reaction/240374

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-Benzyl-4-piperidinolHCID 98152—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물3-Methyl-5-(pyridin-4-yl)-1,2-oxazole-4-carboxylic acidHCID 28275767—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물(4-Benzyl-4-hydroxypiperidin-1-yl)(3-methyl-5-(pyridin-4-yl)-1,2-oxazol-4-yl)methanoneHCID 8668084562.8%

반응 단계

A suspension of 3-methyl-5-(pyridin-4-yl)-1,2-oxazole-4-carboxylic acid (0.25 g), 4-benzyl-4-hydroxypiperidine (0.35 g), HATU (0.70 g) and triethylamine (0.85 mL) in DMF (5.0 mL) was stirred at room temperature for 3 hr. The reaction mixture was diluted with water, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane), and then purified by preparative HPLC(C18, mobile phase: water/acetonitrile (containing 0.1% TFA)), and the obtained fraction was concentrated under reduced pressure. To the residue was added saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure to give the title compound (0.29 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08648079B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-b0b798eea0d54ee49d2273620a0ec98b
출처 메모uspto-grants-2014_02