반응식
[Cl:1][C:2]1[CH:3]=[C:4](/[C:9](=[CH:13]\[C:14]2C=CC=CC=2)/[C:10](O)=O)[CH:5]=[CH:6][C:7]=1[OH:8].CN(C([O:27][N:28]1N=N[C:30]2[CH:31]=[CH:32][CH:33]=N[C:29]1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C.Cl.N[OH:55]>CN(C=O)C>[Cl:1][C:2]1[CH:3]=[C:4]([C:9]2[CH:10]=[CH:33][C:32](/[CH:31]=[CH:30]/[C:29]([NH:28][OH:27])=[O:55])=[CH:14][CH:13]=2)[CH:5]=[CH:6][C:7]=1[OH:8]참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
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).
후처리
- customthe solution thus obtained
- stirringthe mixture was stirred at room temperature for 2 days
- customDMF was removed under reduced pressure
- washthe residue was washed with water
- customto obtain
- filtrationafter filtration, 140 mg of a crude product
- customPurification by flash chromatography on reverse phase ((LiChroprep RP-18, MERCK)
- customwater/methanol 1:1 and crystallization from diethyl ether
출처 및 근거
- ORD 기록
- ord-4f92bbdf0eb249bf94c24643ff3d3a30
- 출처 데이터셋
- uspto-grants-2010_06
- 특허 번호
- US07728039B2
연결된 노트
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