反応式
[F:1][C:2]1[CH:10]=[CH:9][C:5]([C:6](O)=[O:7])=[CH:4][C:3]=1[C:11]1[CH:12]=[C:13]([CH:21]([CH3:23])[CH3:22])[CH:14]=[C:15]2[C:20]=1[N:19]=[CH:18][CH:17]=[CH:16]2.CCN=C=NCCCN(C)C.[NH2:35][C:36]1[N:37]([CH3:42])[CH2:38][C:39](=[O:41])[N:40]=1>CN(C1C=CN=CC=1)C.C(Cl)Cl.C([O-])(O)=O.[Na+]>[F:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([NH:35][C:36]2[N:37]([CH3:42])[CH2:38][C:39](=[O:41])[N:40]=2)=[O:7])=[CH:4][C:3]=1[C:11]1[CH:12]=[C:13]([CH:21]([CH3:22])[CH3:23])[CH:14]=[C:15]2[C:20]=1[N:19]=[CH:18][CH:17]=[CH:16]2参加物
7
反応物 3
生成物 1
試薬・触媒・溶媒 3
実験手順
To solution of the 4-fluoro-3-(6-isopropyl-quinolin-8-yl)-benzoic acid from Step 2 (1.0 eq), EDCI (1.1 eq) and DMAP (1.1 eq) in CH2Cl2 (0.07M) was added 2-amino-1-methyl-1,5-dihydro-imidazol-4-one (1.1 eq). The resulting mixture was stirred for 12 h, poured in saturated aqueous NaHCO3 and extracted with EtOAc (2×). The combined organic extracts were washed with brine, dried over MgSO4, filtered and concentrated. Flash chromatography (EtOAc) afforded the compound as a white solid.
後処理
- extractionextracted with EtOAc (2×)
- washThe combined organic extracts were washed with brine
- dry with materialdried over MgSO4
- filtrationfiltered
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-a44bb52dd197423984a41fcf35bb74e5
- 出典データセット
- uspto-grants-2006_12
- 特許番号
- US07144896B2
関連ノート
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