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Cyclohexanone → 8-[4-(1-Cyano-cyclohexyl)-piperazin-1-yl]-9-ethyl-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile

HRID 2275246
ノート
印刷プレビュー

反応式

HRID 2275246 の反応式
[CH2:1]([C:3]1[C:24]([N:25]2[CH2:30][CH2:29][NH:28][CH2:27][CH2:26]2)=[CH:23][C:6]2[C:7]([CH3:22])([CH3:21])[C:8]3[NH:9][C:10]4[C:15]([C:16]=3[C:17](=[O:18])[C:5]=2[CH:4]=1)=[CH:14][CH:13]=[C:12]([C:19]#[N:20])[CH:11]=4)[CH3:2].[C:31]1(=O)[CH2:36][CH2:35][CH2:34][CH2:33][CH2:32]1.C[Si]([C:42]#[N:43])(C)C>C(Cl)(Cl)Cl.C(OCC)(=O)C.[I-].[Zn+2].[I-]>[C:42]([C:31]1([N:28]2[CH2:29][CH2:30][N:25]([C:24]3[C:3]([CH2:1][CH3:2])=[CH:4][C:5]4[C:17](=[O:18])[C:16]5[C:15]6[C:10](=[CH:11][C:12]([C:19]#[N:20])=[CH:13][CH:14]=6)[NH:9][C:8]=5[C:7]([CH3:22])([CH3:21])[C:6]=4[CH:23]=3)[CH2:26][CH2:27]2)[CH2:36][CH2:35][CH2:34][CH2:33][CH2:32]1)#[N:43]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

HCID 7967CyclohexanoneHCID 82115Trimethylsilyl cyanideHCID 66834254HCID 66834254、化合物

生成物 1

HCID 668349718-[4-(1-Cyano-cyclohexyl)-piperazin-1-yl]-9-ethyl-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile収率 30%

試薬・触媒・溶媒 3

HCID 9883512zinc(II)iodide触媒
HCID 6212
Chloroform
溶媒
HCID 8857Ethyl Acetate溶媒

反応条件

温度
60 °C

実験手順

9-Ethyl-6,6-dimethyl-11-oxo-8-piperazin-1-yl-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile (45 mg) and cyclohexanone (25 mg) were suspended in chloroform (2 ml), added with trimethylsilyl cyanide (30 mg) and zinc iodide (5 mg), and the mixture was stirred at 60° C. for 17 hrs. The reaction mixture was diluted with ethyl acetate (20 ml) and the organic layer was washed with 10% brine solution and concentrated under reduced pressure. The resulting residues were purified by silica gel column (dichloromethane/methanol (=99/1)) to obtain the title compound (12 mg, yield 30%).

後処理

  1. washthe organic layer was washed with 10% brine solution
  2. concentrationconcentrated under reduced pressure
  3. customThe resulting residues were purified by silica gel column (dichloromethane/methanol (=99/1))

出典と根拠

ORDレコード
ord-c14ed9213fd14209abc26bc49f833c96
出典データセット
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09126931B2

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート