Methanol → HCID 178493460、化合物
反応式
COC1C=CC(CN2CCN(CC3N=CC([NH:21][C:22]([C:24]4[CH:25]=[CH:26][C:27]([C:34]5[C:39]([Cl:40])=[C:38]([O:41][CH3:42])[CH:37]=[C:36]([O:43][CH3:44])[C:35]=5[Cl:45])=[C:28]5[C:33]=4[N:32]=[CH:31][CH:30]=[CH:29]5)=[O:23])=CC=3)CC2)=CC=1.[CH3:48][N:49]([CH3:59])[CH2:50][C:51]1[N:52]=[C:53]([N+]([O-])=O)[NH:54][CH:55]=1.CO.C1COCC1.CO>[Ni].C(Cl)Cl.CO>[CH3:48][N:49]([CH2:50][C:51]1[N:52]=[C:53]([NH:21][C:22]([C:24]2[CH:25]=[CH:26][C:27]([C:34]3[C:39]([Cl:40])=[C:38]([O:41][CH3:42])[CH:37]=[C:36]([O:43][CH3:44])[C:35]=3[Cl:45])=[C:28]3[C:33]=2[N:32]=[CH:31][CH:30]=[CH:29]3)=[O:23])[NH:54][CH:55]=1)[CH3:59]参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
The title compound was prepared in analogy to the procedures described in Example 14 but using 5-(2,6-dichloro-3,5-dimethoxy-phenyl)-quinoline-8-carboxylic acid (6-piperazin-1-ylmethyl-pyridin-3-yl)-amide (Example 170), dimethyl-(2-nitro-1H-imidazol-4-ylmethyl)-amine (Step 22.1) instead of 2-nitroimidazole in Step 14.3, and Raney nickel and MeOH/THF (1:1) instead of palladium on carbon and MeOH in Step 14.2. The title compound: ESI-MS: 500.0 [M+H]+; tR=3.50 min (System 1); TLC: Rf=0.20 (DCM/MeOH, 9:1).
後処理
- customThe title compound was prepared in analogy to the procedures
出典と根拠
- ORDレコード
- ord-83706f7f10c64d35bc935460e316751d
- 出典データセット
- uspto-grants-2014_03
- 特許番号
- US08674099B2
反応ノート
読み込み中…