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1,3-Dibromopropane → HCID 66728202, 화합물

HRID 573304
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HRID 573304 반응식
[CH3:1][O:2][CH2:3][O:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]2[C:15]3=[N:16][CH:17]=[CH:18][CH:19]=[C:14]3[NH:13][CH:12]=2)=[CH:7][CH:6]=1.[H-].[Na+].[Br:22][CH2:23][CH2:24][CH2:25]Br>O>[Br:22][CH2:23][CH2:24][CH2:25][N:13]1[C:14]2[C:15](=[N:16][CH:17]=[CH:18][CH:19]=2)[C:11]([C:8]2[CH:7]=[CH:6][C:5]([O:4][CH2:3][O:2][CH3:1])=[CH:10][CH:9]=2)=[CH:12]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 80011,3-DibromopropaneHCID 24758Sodium hydrideHCID 66727950HCID 66727950, 화합물

생성물 1

HCID 66728202HCID 66728202, 화합물

시약·촉매·용매 1

HCID 962Water용매

실험 절차

To a solution of 3-[4-(methoxymethoxy)phenyl]-1H-pyrrolo[3,2-b]pyridine (650 mg) was added NaH (60% in oil, 153 mg) at 0° C. After stirring at room temperature for 1 h, the mixture was added dropwise to 1,3-dibromopropane (0.778 mL). The mixture was stirred at room temperature for 2 h. The mixture was added to water and extracted with AcOEt. The organic layer was washed with brine, dried over Na2SO4 and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (AcOEt/hexane) to give the title compound (486 mg).

후처리

  1. stirringThe mixture was stirred at room temperature for 2 h
  2. extractionextracted with AcOEt
  3. washThe organic layer was washed with brine
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was purified by silica gel column chromatography (AcOEt/hexane)

출처 및 근거

ORD 기록
ord-d97080c5c41d47ec802dc3dd8b860d90
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09029536B2

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