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2-Methoxyethylamine → 2-(4-Bromo-1H-pyrazol-1-yl)-N-(2-methoxyethyl)ethanamine

HRID 1952451
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HRID 1952451 반응식
[CH3:1][O:2][CH2:3][CH2:4][NH2:5].[Br:6][C:7]1[CH:8]=[N:9][N:10]([CH2:12][CH2:13]Cl)[CH:11]=1>CS(C)=O.CCOC(C)=O>[Br:6][C:7]1[CH:8]=[N:9][N:10]([CH2:12][CH2:13][NH:5][CH2:4][CH2:3][O:2][CH3:1])[CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 80182-MethoxyethylamineHCID 518920744-bromo-1-(2-chloroethyl)-1H-pyrazole

생성물 1

HCID 625656882-(4-Bromo-1H-pyrazol-1-yl)-N-(2-methoxyethyl)ethanamine수율 100%

시약·촉매·용매 2

HCID 679Dimethyl Sulfoxide용매HCID 8857Ethyl Acetate용매

실험 절차

A solution of 2-methoxyethanamine (8.9 mL, 102.06 mmol) and chloride 75 (7.13 g, 34.02 mmol) in DMSO (20 mL) was heated at 60° C. 5 h. The mixture was then cooled to room temperature, diluted with EtOAc, washed with aqueous sodium bicarbonate, water and brine. The organic phase was further extracted with 1N HCl and the acid extract was collected and basified with 2N NaOH (pH˜11). The basic aqueous solution was extracted with DCM, the DCM extract was dried over anhydrous sodium sulphate, and concentrated under reduced pressure to afford title compound 76 (8.44 g, 99%) as brown foam. MS (m/z): 248.04 (M+H).

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후처리

  1. custom5 h
  2. washwashed with aqueous sodium bicarbonate, water and brine
  3. extractionThe organic phase was further extracted with 1N HCl
  4. extractionthe acid extract
  5. customwas collected
  6. extractionThe basic aqueous solution was extracted with DCM
  7. extractionthe DCM extract
  8. dry with materialwas dried over anhydrous sodium sulphate
  9. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-ffe0cf69d4214af0ba3b7e69bf95f282
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08404846B2

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