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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12989생성일: 2026년 10월 24일

Diisopropylethylamine → E-3-[3'-chloro-4'-hydroxybiphenyl-4-yl]-N-hydroxy-acrylamide

https://huagongshe.com/ko/reaction/12989

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Hydroxyamine hydrochlorideHCID 443297—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물E-3-chloro-4-hydroxyphenylcinnamic acidHCID 68583309—
용매DimethylformamideHCID 6228—
생성물E-3-[3'-chloro-4'-hydroxybiphenyl-4-yl]-N-hydroxy-acrylamideHCID 159865079.7%

반응 단계

205 mg (0.75 mmol) of E-3-chloro-4-hydroxyphenylcinnamic acid were dissolved under nitrogen in 7.5 ml of DMF, then 285 mg (0.75 mmol) of HATU and 97 μL (0.56 mmol) of DIPEA were added and the solution thus obtained was kept under stirring at room temperature for 2 min. After addition of hydroxylamine hydrochloride (261 mg, 3.75 mmol), the mixture was stirred at room temperature for 2 days. DMF was removed under reduced pressure and the residue was washed with water to obtain, after filtration, 140 mg of a crude product. Purification by flash chromatography on reverse phase ((LiChroprep RP-18, MERCK) using as eluent water/methanol 1:1 and crystallization from diethyl ether afforded 21 mg of the title compound as a white solid. M.p. 172-175° C. Rf=0.16 (RP18 MERCK, H2O/MeOH 1:1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728039B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-4f92bbdf0eb249bf94c24643ff3d3a30
출처 메모uspto-grants-2010_06