Ammonium Chloride → 4',5'-Diamino-2'-fluorobiphenyl-4-carbonitrile

HRID 1424218ノート

反応式

HRID 1424218 の反応式
[NH2:1][C:2]1[C:7]([N+:8]([O-])=O)=[CH:6][C:5]([C:11]2[CH:16]=[CH:15][C:14]([C:17]#[N:18])=[CH:13][CH:12]=2)=[C:4]([F:19])[CH:3]=1.[Cl-].[NH4+]>CO.[Zn]>[NH2:1][C:2]1[C:7]([NH2:8])=[CH:6][C:5]([C:11]2[CH:12]=[CH:13][C:14]([C:17]#[N:18])=[CH:15][CH:16]=2)=[C:4]([F:19])[CH:3]=1

参加物

5

反応物 2

HCID 25517Ammonium ChlorideHCID 866991314'-Amino-2'-fluoro-5'-nitrobiphenyl-4-carbonitrile

生成物 1

HCID 866990294',5'-Diamino-2'-fluorobiphenyl-4-carbonitrile収率 99%

試薬・触媒・溶媒 2

HCID 23994Zinc触媒HCID 887Methanol溶媒

実験手順

To a mixture of 4′-amino-2′-fluoro-5′-nitrobiphenyl-4-carbonitrile (Preparation 90, 0.5 g, 2 mmol) and zinc dust (0.78 g, 12 mmol) in methanol (10 mL) was added ammonium chloride (0.41 g, 8 mmol) and the reaction was stirred at room temperature for 3 hours. The reaction was filtered through celite washing through with methanol (40 mL). The filtrate was concentrated to afford a solid that was purified using silica gel column chromatography eluting with EtOAc:heptanes 1:1 to afford the title compound as a brown solid (0.45 g, 99%).

後処理

  1. filtrationThe reaction was filtered through celite
  2. washwashing through with methanol (40 mL)
  3. concentrationThe filtrate was concentrated
  4. customto afford a solid
  5. customthat was purified
  6. washeluting with EtOAc:heptanes 1:1

出典と根拠

ORDレコード
ord-08a34fe16450434993d349b60e5c6014
出典データセット
uspto-grants-2015_01
特許番号
US08927587B2

反応ノート

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