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

HRID 230636
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HRID 230636 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

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

생성물 1

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

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-a38f9db399a94e7590119daaa674b8c7
출처 데이터셋
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07566735B2

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