1-Methyl-1H-imidazole-5-carbonitrile → 2-(8-Hydroxy-2-methyl-quinolin-4-yl)-3-methyl-3H-imidazole-4-carbonitrile
反応式
Br[C:2]1[C:11]2[C:6](=[C:7]([OH:12])[CH:8]=[CH:9][CH:10]=2)[N:5]=[C:4]([CH3:13])[CH:3]=1.[CH3:14][N:15]1[C:19]([C:20]#[N:21])=[CH:18][N:17]=[CH:16]1.CC1C=C(C2N(C)C=CN=2)C2C(=C(O)C=CC=2)N=1>>[OH:12][C:7]1[CH:8]=[CH:9][CH:10]=[C:11]2[C:6]=1[N:5]=[C:4]([CH3:13])[CH:3]=[C:2]2[C:16]1[N:15]([CH3:14])[C:19]([C:20]#[N:21])=[CH:18][N:17]=1参加物
4
実験手順
Coupling of 4-bromo-2-methyl-quinolin-8-ol (400 mg. 1.68 mmol) with 3-methyl-3H-imidazole-4-carbonitrile (450 mg. 4.20 mmol) according to the synthesis of 2-methyl-4-(1-methyl-1H-imidazol-2-yl)-quinolin-8-ol yielded the title compound. MS (m/z): 265.2 [M+H+].
出典と根拠
- ORDレコード
- ord-bd625cb49dc9408fb5181df0dd466ede
- 出典データセット
- uspto-grants-2013_04
- 特許番号
- US08410134B2
反応ノート
読み込み中…