HCID 178526787、化合物 → HCID 178508009、化合物

HRID 506586ノート

反応式

HRID 506586 の反応式
[N+:1]([C:4]1[CH:5]=[C:6]2[N:12]=[C:11]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[NH:10][C:7]2=[N:8][CH:9]=1)([O-])=O>C(O)(=O)C.[Fe]>[C:13]1([C:11]2[NH:10][C:7]3=[N:8][CH:9]=[C:4]([NH2:1])[CH:5]=[C:6]3[N:12]=2)[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1

参加物

4

反応物 1

HCID 178526787HCID 178526787、化合物

生成物 1

HCID 178508009HCID 178508009、化合物

試薬・触媒・溶媒 2

HCID 23925Iron触媒HCID 176Acetic Acid溶媒

反応条件

温度
80 °C

実験手順

12.0 g 6-nitro-2-phenyl-3H-imidazo[4,5-b]pyridine were dissolved in 1 l acetic acid. 18 g iron powder were added and the mixture heated to 80° C. with stirring. After 2 hrs the mixture was cooled to room temperature and filtered over Celite. The celite pad was washed with methanol and the combined filtrates were evaporated. The residue was dissolved methanol/dichloromethane 1:1 and filtered over silica. The filtrate was concentrated to a volume of 100 ml, the resulting precipitate collected by filtration and washed with methanol.

後処理

  1. temperatureAfter 2 hrs the mixture was cooled to room temperature
  2. filtrationfiltered over Celite
  3. washThe celite pad was washed with methanol
  4. customthe combined filtrates were evaporated
  5. dissolutionThe residue was dissolved methanol/dichloromethane 1:1
  6. filtrationfiltered over silica
  7. concentrationThe filtrate was concentrated to a volume of 100 ml
  8. filtrationthe resulting precipitate collected by filtration
  9. washwashed with methanol

出典と根拠

ORDレコード
ord-7eccfa8a6b064489a8be3fe27790677f
出典データセット
uspto-grants-2010_08
特許番号
US07786113B2

反応ノート

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