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Methyl iodide → N-[(4-bromophenyl)methyl]-N-methyl-1-pyrrolidinecarboxamide

HRID 230636
ノート
印刷プレビュー

反応式

HRID 230636 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][NH:9][C:10]([N:12]2[CH2:16][CH2:15][CH2:14][CH2:13]2)=[O:11])=[CH:4][CH:3]=1.[H-].[Na+].I[CH3:20]>CN(C)C=O>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][N:9]([CH3:20])[C:10]([N:12]2[CH2:16][CH2:15][CH2:14][CH2:13]2)=[O:11])=[CH:4][CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 57762826N-[(4-bromophenyl)methyl]-1-pyrrolidinecarboxamide

生成物 1

HCID 57762825N-[(4-bromophenyl)methyl]-N-methyl-1-pyrrolidinecarboxamide収率 103.9%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

N-[(4-bromophenyl)methyl]-1-pyrrolidinecarboxamide (230 mg, 0.81 mmol), was dissolved in dimethylformamide (2 ml) and treated at room temperature with a 60% sodium hydride suspension in mineral oil (33 mg, 0.83 mmol). This mix was stirred for 15 minutes before being treated with iodomethane (116 mg, 0.82 mmol). The resulting mix was stirred at 20° C. for a total of 16.5 hours. The reaction was quenched with water (4 ml) and extracted into ethyl acetate (4 ml). The organic layer was dried over sodium sulphate and the solvent removed under reduced pressure to give the title compound as a colourless oil (250 mg, crude). LC/Mass Spec (ES): Found 297 (ES+), retention time 2.90 mins. C13H1779BrN2O requires 296.

後処理

  1. additionThe resulting mix
  2. stirringwas stirred at 20° C. for a total of 16.5 hours
  3. customThe reaction was quenched with water (4 ml)
  4. extractionextracted into ethyl acetate (4 ml)
  5. dry with materialThe organic layer was dried over sodium sulphate
  6. customthe solvent removed under reduced pressure

出典と根拠

ORDレコード
ord-a38f9db399a94e7590119daaa674b8c7
出典データセット
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07566735B2

反応ノート

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