Ethanol → 4-Amino-5-(4-hydroxy-phenylsulfanyl)-thiophene-2-carboxylic acid (3-bromo-phenyl)-amide

HRID 605314ノート

反応式

HRID 605314 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([NH:8][C:9]([C:11]2[S:12][C:13]([S:19][C:20]3[CH:25]=[CH:24][C:23]([OH:26])=[CH:22][CH:21]=3)=[C:14]([N+:16]([O-])=O)[CH:15]=2)=[O:10])[CH:5]=[CH:6][CH:7]=1.[Cl-].[NH4+].O.C(O)C>O1CCCC1.[Fe]>[Br:1][C:2]1[CH:3]=[C:4]([NH:8][C:9]([C:11]2[S:12][C:13]([S:19][C:20]3[CH:21]=[CH:22][C:23]([OH:26])=[CH:24][CH:25]=3)=[C:14]([NH2:16])[CH:15]=2)=[O:10])[CH:5]=[CH:6][CH:7]=1

参加物

7

反応物 4

HCID 702EthanolHCID 962WaterHCID 25517Ammonium ChlorideHCID 670409995-(4-Hydroxy-phenylsulfanyl)-4-nitro-thiophene-2-carboxylic acid (3-bromo-phenyl)-amide

生成物 1

HCID 670406504-Amino-5-(4-hydroxy-phenylsulfanyl)-thiophene-2-carboxylic acid (3-bromo-phenyl)-amide

試薬・触媒・溶媒 2

HCID 23925Iron触媒HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of the product from Example 351D (1 equiv), iron powder (5 equiv) and ammonium chloride (3 equiv) in a mixture of tetrahydrofuran, water and ethanol was heated to reflux for 3 hours. The mixture was cooled to room temperature, filtered through a pad of celite, which was washed with ethanol and the resultant filtrate concentrated under vacuum. The material was then dissolved in water and extracted with ethyl acetate, the organic layer dried and concentrated under vacuum to provide the title product.

後処理

  1. temperaturewas heated
  2. temperatureto reflux for 3 hours
  3. filtrationfiltered through a pad of celite, which
  4. washwas washed with ethanol
  5. concentrationthe resultant filtrate concentrated under vacuum
  6. dissolutionThe material was then dissolved in water
  7. extractionextracted with ethyl acetate
  8. customthe organic layer dried
  9. concentrationconcentrated under vacuum

出典と根拠

ORDレコード
ord-0361d5052b0649b5a41e21c17847411b
出典データセット
uspto-grants-2011_03
特許番号
US07910595B2

反応ノート

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