8-Hydroxyquinoline → HCID 24760755, 화합물

HRID 1802604노트

반응식

HRID 1802604 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=[S:14])=[CH:4][CH:3]=1.[Cl:15][C:16]1[S:20][C:19]([C:21]([NH:23][CH2:24][C:25]2[N:26]=[CH:27][NH:28][CH:29]=2)=[O:22])=[CH:18][CH:17]=1.OC1C=CC=C2C=1N=CC=C2.C([O-])([O-])=O.[K+].[K+]>CS(C)=O.[Cu]I>[Cl:15][C:16]1[S:20][C:19]([C:21]([NH:23][CH2:24][C:25]2[N:26]=[CH:27][N:28]([C:2]3[CH:7]=[CH:6][C:5]([N:8]4[CH:13]=[CH:12][CH:11]=[CH:10][C:9]4=[S:14])=[CH:4][CH:3]=3)[CH:29]=2)=[O:22])=[CH:18][CH:17]=1

참가 물질

7

반응 조건

온도
130 °C

실험 절차

A mixture of 1-(4-iodophenyl)pyridine-2(1H)-thione prepared above (65 mg, 0.21 mmol), 5-chloro-N-((1H-imidazol-4-yl)methyl)thiophene-2-carboxamide 3-1 prepared in Example 11 (65 mg, 0.18 mmol), 8-hydroxyquinoline (10 mg, 0.069 mmol) and K2CO3 (75 mg, 0.54 mmol) in DMSO (2 mL) was degassed with Ar before being charged with CuI (27 mg, 0.14 mmol). The mixture in a sealed tube was heated at 130° C. overnight. It was then purified by HPLC to give the title compound (15 mg). MS 427.0 and 429.0 (M+H, Cl pattern).

후처리

  1. customwas degassed with Ar
  2. customIt was then purified by HPLC

출처 및 근거

ORD 기록
ord-bc7fc4be86324fe9ac70b6924114d3dd
출처 데이터셋
uspto-grants-2013_01
특허 번호
US08349873B2

반응 노트

불러오는 중…