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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 619503생성일: 2026년 10월 26일

Triethylamine → 4,5-dihydro-4-(1-pentafluoropropionylpiperidin-4-ylmethyl)-3H-1,4,8b-triazaacenaphthylen-3-one

https://huagongshe.com/reaction/619503

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Pentafluoropropionic anhydrideHCID 67742—
반응물4,5-dihydro-4-(piperidin-4-ylmethyl)-3H-1,4,8b-triazaacenaphthylen-3-one dihydrochlorideHCID 21190271—
용매AcetonitrileHCID 6342—
생성물4,5-dihydro-4-(1-pentafluoropropionylpiperidin-4-ylmethyl)-3H-1,4,8b-triazaacenaphthylen-3-oneHCID 2119018763.2%

반응 단계

In 10 ml of acetonitrile was suspended 687 mg (2.0 mM) of 4,5-dihydro-4-(piperidin-4-ylmethyl)-3H-1,4,8b-triazaacenaphthylen-3-one dihydrochloride, followed by addition of 2.23 ml (16.0 mM) of triethylamine and 1.97 ml (10.0 mM) of pentafluoropropionic anhydride in the order mentioned. This mixture was stirred at room temperature for 1 hour and the solvent was then distilled off under reduced pressure. The residue was extracted with 50 ml of chloroform and the organic layer was washed with 50 ml of saturated aqueous NaCl solution and dried over MgSO4. The solvent was distilled off under reduced pressure and the residue was purified by silica gel column chromatography (eluent: ethyl acetate-ethanol=10:1) to provide 526 mg (yield 63.2%) of the title compound as light-yellow amorphous substance.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05958942
출처 데이터셋uspto-grants-1999_09
ORD IDord-0252bce3457644bbbb16f94f784aa001
출처 메모uspto-grants-1999_09