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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 736114생성일: 2026년 10월 25일

Triethylamine → 1-{3-Fluoro-4-[4-(2-fluoro-5-nitrobenzoyl)piperazino]phenyl}-1-ethanone

https://huagongshe.com/reaction/736114

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-(3-Fluoro-4-piperazin-1-ylphenyl)ethanoneHCID 685610—
반응물2-Fluoro-5-nitrobenzoyl chlorideHCID 10976570—
용매1,4-DioxaneHCID 31275—
생성물1-{3-Fluoro-4-[4-(2-fluoro-5-nitrobenzoyl)piperazino]phenyl}-1-ethanoneHCID 136226768%

반응 단계

A solution of 2-Fluoro-5-nitro-benzoyl chloride (CAS: 7304-32-7; Feng, Y.; Burgess, K.; Chem. Europ. J.; EN; 5; 11; 1999; 3261-3272) (0.054 g, 0.261 mmol) in dioxane (1 ml) was treated with triethylamine (0.073 ml, 0.522 mmol) and then with a solution of 1-(3-Fluoro-4-piperazin-1-yl-phenyl)-ethanone (CAS: 189763-57-3; WO9714690) (58 mg, 0.261 mmol) in dioxane (1 ml). The mixture was stirred at room temperature for 30 minutes. The solvent was removed in vacuo. The crude oil was taken in water. The aqueous layer was extracted 3 times with CH2Cl2. The combined extracts were dried over Na2SO4, filtered and the solvent was removed in vacuo. The crude gum was purified on silicagel (eluent: heptane/ethylacetate 0%-20% (10 minutes) to provide the title compound (69 mg, 68%) as a light yellow solid, MS (m/e): 390.2 (MH+, 100%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07595314B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-e081220ca2134026ba3c0b5f80a6bfe0
출처 메모uspto-grants-2009_09