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Carbazole → 9-(5-bromopyridin-3-yl)-9H-carbazole

HRID 520826
ノート
印刷プレビュー

反応式

HRID 520826 の反応式
[CH:1]1[C:13]2[NH:12][C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:5]=2[CH:4]=[CH:3][CH:2]=1.[Br:14][C:15]1[CH:16]=[N:17][CH:18]=[C:19](Br)[CH:20]=1.C(=O)([O-])[O-].[K+].[K+].C1OCCOCCOCCOCCOCCOC1>CN(C=O)C.[Cu]>[Br:14][C:15]1[CH:20]=[C:19]([N:12]2[C:11]3[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=3[C:5]3[C:13]2=[CH:1][CH:2]=[CH:3][CH:4]=3)[CH:18]=[N:17][CH:16]=1
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 4

HCID 6854CarbazoleHCID 11430Potassium CarbonateHCID 2855718-Crown-6HCID 693693,5-Dibromopyridine

生成物 1

HCID 594495909-(5-bromopyridin-3-yl)-9H-carbazole収率 60%

試薬・触媒・溶媒 2

HCID 23978Copper触媒
HCID 6228
Dimethylformamide
溶媒

反応条件

温度
150 °C

実験手順

A mixture of 9H-carbazole (4.0 g, 24.1 mmol), 3,5-dibromopyridine (8.55 g, 36.1 mmol), copper powder (3.06 g, 48.2 mmol), potassium carbonate (13.3 g, 96.4 mmol) and 18-crown-6 (0.636 g, 2.4 mmol) in anhydrous DMF was degassed and heated at about 150° C. for about 40 hours. The crude mixture was then poured into water (200 mL), and then filtered. The solid was collected and dissolved in hot dichloromethane (500 mL) and an insoluble solid was then filtered off. The solution was absorbed on silica gel and purified by flash column (hexanes/ethyl acetate 12:1) to give a white solid product 2B (4.67 g, yield: 60%).

後処理

  1. customwas degassed
  2. additionThe crude mixture was then poured into water (200 mL)
  3. filtrationfiltered
  4. customThe solid was collected
  5. dissolutiondissolved in hot dichloromethane (500 mL)
  6. filtrationan insoluble solid was then filtered off
  7. customThe solution was absorbed on silica gel
  8. custompurified by flash column (hexanes/ethyl acetate 12:1)

出典と根拠

ORDレコード
ord-d47d54d78e7a428fab7fa25bd0e9e728
出典データセット
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09328094B2

反応ノート

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