Dimethylamine → N,N-dimethyl-1-(2-methyl-4-nitro-1H-indol-3-yl)methanamine

HRID 12620ノート

反応式

HRID 12620 の反応式
[CH2:1]=O.[CH3:3][NH:4][CH3:5].[CH3:6][C:7]1[NH:8][C:9]2[C:14]([CH:15]=1)=[C:13]([N+:16]([O-:18])=[O:17])[CH:12]=[CH:11][CH:10]=2.[OH-].[Na+]>C(O)(=O)C>[CH3:3][N:4]([CH3:1])[CH2:5][C:15]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][C:13]=2[N+:16]([O-:18])=[O:17])[NH:8][C:7]=1[CH3:6]

参加物

6

反応物 4

HCID 674DimethylamineHCID 712FormaldehydeHCID 14798Sodium HydroxideHCID 110951501H-Indole, 2-methyl-4-nitro-

生成物 1

HCID 68689213N,N-dimethyl-1-(2-methyl-4-nitro-1H-indol-3-yl)methanamine

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒2 回

実験手順

To an acetic acid (5 mL) solution of an aqueous 370% formaldehyde solution (271 mg), an aqueous 50% dimethylamine solution (317 mg) was slowly added dropwise under ice cooling and the mixture was stirred at room temperature for 30 minutes. Furthermore, an acetic acid (1 mL) solution of 2-methyl-4-nitro-1H-indole [Tetrahedron 1, 1999, 5395-5398] (310 mg) was added and the mixture was stirred at room temperature for 24 hours. The pH of the reaction mix was adjusted to 9 using an aqueous 5M sodium hydroxide solution, followed by extraction with dichloromethane three times. The organic layer was washed with saturated saline, dried over anhydrous sodium sulfate and then concentrated. The residue was washed with diisopropyl ether to obtain the titled compound having the following physical properties (303 mg).

後処理

  1. stirringthe mixture was stirred at room temperature for 24 hours
  2. additionThe pH of the reaction mix
  3. extractionfollowed by extraction with dichloromethane three times
  4. washThe organic layer was washed with saturated saline
  5. dry with materialdried over anhydrous sodium sulfate
  6. concentrationconcentrated
  7. washThe residue was washed with diisopropyl ether

出典と根拠

ORDレコード
ord-3e013e4fe1c942929986588c683791e1
出典データセット
uspto-grants-2010_06
特許番号
US07728023B2

反応ノート

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