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Dimethylformamide → Methyl 6-bromo-1-methyl-1H-indole-3-carboxylate

HRID 424785
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인쇄 미리보기

반응식

HRID 424785 반응식
COC(C1[C:13]2[C:8](=[CH:9][CH:10]=[C:11]([Br:14])[CH:12]=2)NC=1)=O.[C:15](=[O:18])([O-])[O-:16].[K+].[K+].I[CH3:22].[CH3:23][N:24]([CH:26]=O)[CH3:25]>ClCCl>[CH3:22][O:16][C:15]([C:13]1[C:8]2[C:23](=[CH:12][C:11]([Br:14])=[CH:10][CH:9]=2)[N:24]([CH3:25])[CH:26]=1)=[O:18]
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참가 물질

6

반응물 4

HCID 6228DimethylformamideHCID 6328Methyl iodide2회HCID 11430Potassium CarbonateHCID 285091Methyl 5-bromo-1H-indole-3-carboxylate

생성물 1

HCID 57443279Methyl 6-bromo-1-methyl-1H-indole-3-carboxylate수율 99%

시약·촉매·용매 1

HCID 6344
Dichloromethane
용매

실험 절차

To a mixture of 5-bromo-1H-indole-3-carboxylic acid methyl ester (100 mg, 0.394 mmol), potassium carbonate (163 mg, 1.18 mmol) in DMF is added iodomethane (30 μL, 0.47 mmol). The reaction mixture is stirred for 1.5 hours. Additional iodomethane (10 μL) is added and the reaction is stirred for 30 minutes. The reaction mixture is diluted with dichloromethane and filtered. The filtrate is concentrated under high vacuum, diluted with ethyl acetate, and concentrated to give 105 mg (99%) of the title compound. ES/MS m/e 270.0 (M+2).

후처리

  1. stirringthe reaction is stirred for 30 minutes
  2. filtrationfiltered
  3. concentrationThe filtrate is concentrated under high vacuum
  4. additiondiluted with ethyl acetate
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-3d3510a86f1f4abe8d158c93f33bd81e
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08106077B2

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