Dimethylformamide → 2-(4-Hydroxy-3-methoxy-5-nitrobenzoyl)-3-methylindole

HRID 274464

反応式

HRID 274464 の反応式
Br[CH2:2][C:3]([C:5]1[CH:10]=[C:9]([N+:11]([O-:13])=[O:12])[C:8]([OH:14])=[C:7]([O:15][CH3:16])[CH:6]=1)=[O:4].N[CH2:18][C:19]([C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)=O.C[N:28](C)C=O>>[OH:14][C:8]1[C:9]([N+:11]([O-:13])=[O:12])=[CH:10][C:5]([C:3]([C:2]2[NH:28][C:26]3[C:21]([C:19]=2[CH3:18])=[CH:22][CH:23]=[CH:24][CH:25]=3)=[O:4])=[CH:6][C:7]=1[O:15][CH3:16]

参加物

4

反応物 3

HCID 6228DimethylformamideHCID 11952PhenacylamineHCID 144509832-Bromo-4'-hydroxy-3'-methoxy-5'-nitroacetophenone

生成物 1

HCID 214589792-(4-Hydroxy-3-methoxy-5-nitrobenzoyl)-3-methylindole

実験手順

ac) A solution of 29.0 g of 2-bromo-4'-hydroxy-3'-methoxy-5'-nitroacetophenone and 13.5 g of 2-aminoacetophenone in 250 ml of dry N,N-dimethylformamide is stirred at 90° for 16 hours. The reaction mixture is then evaporated to about two thirds and poured on to ice. The separated crystals are filtered under suction and dissolved in methylene chloride. The solution is washed with saturated sodium chloride solution, dried over sodium sulfate, filtered and evaporated. There is obtained 2-(4-hydroxy-3-methoxy-5-nitrobenzoyl)-3-methylindole of m.p. 195°-197° (from methylene chloride/methanol).

後処理

  1. customThe reaction mixture is then evaporated to about two thirds
  2. additionpoured on to ice
  3. filtrationThe separated crystals are filtered under suction
  4. dissolutiondissolved in methylene chloride
  5. washThe solution is washed with saturated sodium chloride solution
  6. dry with materialdried over sodium sulfate
  7. filtrationfiltered
  8. customevaporated

出典と根拠

ORDレコード
ord-9b3c989b9113448f9692f78581fca85a
出典データセット
uspto-grants-1995_02
特許番号
US05389653

関連ノート

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