8-Hydroxyquinoline → HCID 178512036, 화합물
반응식
I[C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH:13]=[CH:12][CH:11]=[CH:10]/[C:9]/2=[N:14]\[C:15]#[N:16])=[CH:4][CH:3]=1.[Cl:17][C:18]1[S:22][C:21]([C:23]([NH:25][CH2:26][C:27]2[N:28]=[CH:29][NH:30][CH:31]=2)=[O:24])=[CH:20][CH:19]=1.OC1C=CC=C2C=1N=CC=C2.C([O-])([O-])=O.[K+].[K+]>CS(C)=O.[Cu]I>[Cl:17][C:18]1[S:22][C:21]([C:23]([NH:25][CH2:26][C:27]2[N:28]=[CH:29][N:30]([C:2]3[CH:7]=[CH:6][C:5]([N:8]4[CH:13]=[CH:12][CH:11]=[CH:10]/[C:9]/4=[N:14]\[C:15]#[N:16])=[CH:4][CH:3]=3)[CH:31]=2)=[O:24])=[CH:20][CH:19]=1참가 물질
7
반응 조건
- 온도
- 130 °C
실험 절차
A mixture of (E)-(1-(4-iodophenyl)pyridin-2(1H)-ylidene)cyanamide (25 mg, 0.078 mmol), 5-Chloro-N-((1H-imidazol-4-yl)methyl)thiophene-2-carboxamide 3-1 (65 mg, 0.18 mmol), 8-hydroxyquinoline (10 mg, 0.069 mmol) and K2CO3 (75 mg, 0.54 mmol) in DMSO (1 mL) was degassed with Ar before being charged with CuI (15 mg, 0.079 mmol). The mixture in a sealed tube was heated at 130° C. overnight. It was then purified by HPLC to give the titled compound (10 mg). MS 435.1 and 437.0 (M+H, Cl pattern).
후처리
- customwas degassed with Ar
- customIt was then purified by HPLC
출처 및 근거
- ORD 기록
- ord-9f8ee12235a744149a435a2f7e072828
- 출처 데이터셋
- uspto-grants-2010_08
- 특허 번호
- US07767697B2
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