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(E)-3-(4-Bromophenyl)-1-(pyridazin-4-yl)prop-2-en-1-one → HCID 86684795, 화합물

HRID 1527968
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HRID 1527968 반응식
[C:1]1([CH3:9])[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[Mg]Br.[Br:10][C:11]1[CH:16]=[CH:15][C:14](/[CH:17]=[CH:18]/[C:19]([C:21]2[CH:26]=[CH:25][N:24]=[N:23][CH:22]=2)=[O:20])=[CH:13][CH:12]=1>O1CCCC1.[Cu]I>[Br:10][C:11]1[CH:16]=[CH:15][C:14]([CH:17]([C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][C:1]=2[CH3:9])[CH2:18][C:19]([C:21]2[CH:26]=[CH:25][N:24]=[N:23][CH:22]=2)=[O:20])=[CH:13][CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 86684794(E)-3-(4-Bromophenyl)-1-(pyridazin-4-yl)prop-2-en-1-oneHCID 178424303HCID 178424303, 화합물

생성물 1

HCID 86684795HCID 86684795, 화합물수율 64%

시약·촉매·용매 2

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)촉매HCID 8028Tetrahydrofuran용매2회

실험 절차

To a suspension of copper(I) iodide (63.4 mg, 333 μmol) in tetrahydrofuran (10 ml) was added at 0° C. o-tolylmagnesium bromide solution (2 M in diethyl ether, 3.66 ml, 7.33 mmol) to give a light brown suspension. The reaction mixture was stirred at this temperature for 1½ h, then a solution of (E)-3-(4-bromophenyl)-1-(pyridazin-4-yl)prop-2-en-1-one (963 mg, 3.33 mmol) in THF (5.0 ml) was added, then after 1¾ h the reaction mixture was partitioned between sat. aq. ammonium chloride solution and ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate, filtered, and evaporated. Chromatography (SiO2; ethyl acetate/heptane 1:1) afforded the title compound (809 mg, 64%). Light yellow foam; MS: 381.1 [M+H]+.

후처리

  1. customto give a light brown suspension
  2. customafter 1¾ h the reaction mixture was partitioned between sat. aq. ammonium chloride solution and ethyl acetate
  3. washThe organic layer was washed with brine
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. customevaporated

출처 및 근거

ORD 기록
ord-8272fc30a3d9428c966b9ae49b93795c
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09090565B2

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