1-Chloro-2-iodobenzene → 3-(2-Chlorophenyl)-1-(3-(2-(6,7-difluoro-2-quinolinyl)ethenyl)phenyl)-1-propanone
반응식
[F:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[F:12])[N:8]=[C:7]([CH:13]=[CH:14][C:15]1[CH:16]=[C:17]([CH:21]([OH:24])[CH:22]=[CH2:23])[CH:18]=[CH:19][CH:20]=1)[CH:6]=[CH:5]2.[Cl:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][C:27]=1I.[Li+].[Cl-].[Li]OC(C)=O.O.O>CN(C=O)C.CC([O-])=O.CC([O-])=O.[Pd+2]>[Cl:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][C:27]=1[CH2:23][CH2:22][C:21]([C:17]1[CH:18]=[CH:19][CH:20]=[C:15]([CH:14]=[CH:13][C:7]2[CH:6]=[CH:5][C:4]3[C:9](=[CH:10][C:11]([F:12])=[C:2]([F:1])[CH:3]=3)[N:8]=2)[CH:16]=1)=[O:24]참가 물질
7
반응물 4
생성물 1
시약·촉매·용매 2
반응 조건
- 온도
- 100 °C
실험 절차
A mixture of the allylic alcohol of Step 3 (1.214 g, 3.75 mmol), 1-chloro-2-iodobenzene (480 FtL), Pd(OAc)2 (30 mg), LiCl (194 mg), LiOAc.2H2O (995 rag) and Bu4NCI (2.13 g) in 7.5 mL of DMF was degassed under vacuum and heated to 100° C. under N2 for 3 hr. 25% Aq. NH4OAc was then added and the product was extracted in EtOAc, dried over Na2SO4, and purified by flash chromatography with EtOAc: toluene 2.5:97.5. Yield 1.53 g, 94%.
후처리
- customwas degassed under vacuum
- addition25% Aq. NH4OAc was then added
- extractionthe product was extracted in EtOAc
- dry with materialdried over Na2SO4
- custompurified by flash chromatography with EtOAc: toluene 2.5:97.5
출처 및 근거
- ORD 기록
- ord-930cef5125954df69172621cf29c67a1
- 출처 데이터셋
- uspto-grants-1995_08
- 특허 번호
- US05438141
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