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Dimethylformamide → 3-chloro-5-[(5-chloro-1H-indazol-4-yl)oxy]benzonitrile

HRID 505504
ノート
印刷プレビュー

反応式

HRID 505504 の反応式
Br[C:2]1[CH:3]=[C:4]([CH:16]=[C:17]([Cl:19])[CH:18]=1)[O:5][C:6]1[C:14]([Cl:15])=[CH:13][CH:12]=[C:11]2[C:7]=1[CH:8]=[N:9][NH:10]2.[CH3:20][N:21](C=O)C>[C-]#N.[Zn+2].[C-]#N>[Cl:19][C:17]1[CH:18]=[C:2]([CH:3]=[C:4]([O:5][C:6]2[C:14]([Cl:15])=[CH:13][CH:12]=[C:11]3[C:7]=2[CH:8]=[N:9][NH:10]3)[CH:16]=1)[C:20]#[N:21]
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

4

反応物 2

HCID 6228DimethylformamideHCID 568336424-(3-bromo-5-chlorophenoxy)-5-chloro-1H-indazole

生成物 1

HCID 568336433-chloro-5-[(5-chloro-1H-indazol-4-yl)oxy]benzonitrile

試薬・触媒・溶媒 1

HCID 11186Zinc cyanide (Zn(CN)2)触媒

反応条件

温度
90 °C

実験手順

To a suspension of 4-(3-bromo-5-chlorophenoxy)-5-chloro-1H-indazole (40 g, 112 mmol) and zinc cyanide (15.74 g, 134 mmol) in DMF (400 mL) was added palladium tetrakis triphenylphosphine (38.7 g, 33.5 mmol) and heated to 90° C. for 1 hour. After this time, the reaction was cooled to room temperature and partitioned between saturated aq. NH4Cl (500 mL), water (500 mL) and EtOAc (2×1000 mL). The combined extracts were dried over MgSO4, absorbed onto silica gel (200 g) and the solvent removed in vacuo. This solid was purified on a silica gel (1000 g) column (0-10% EtOAc/CH2Cl2) to give the title compound as a white solid. LRMS (M+1)=303.9

後処理

  1. temperatureAfter this time, the reaction was cooled to room temperature
  2. custompartitioned between saturated aq. NH4Cl (500 mL), water (500 mL) and EtOAc (2×1000 mL)
  3. dry with materialThe combined extracts were dried over MgSO4
  4. customabsorbed onto silica gel (200 g)
  5. customthe solvent removed in vacuo
  6. customThis solid was purified on a silica gel (1000 g) column (0-10% EtOAc/CH2Cl2)

出典と根拠

ORDレコード
ord-43a9e2f84f874303ae3a5ec582a6c1ae
出典データセット
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07781454B2

反応ノート

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