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Hydrochloric Acid → 3-(4-methoxyphenyl)-7-phenyl-2-propyl-2H-indazole

HRID 1295043
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HRID 1295043 반응식
Cl[C:2]1[C:10]2[C:6](=[C:7]([C:14]3[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[CH:16][CH:15]=3)[N:8]([CH2:11][CH2:12][CH3:13])[N:9]=2)[CH:5]=[CH:4][CH:3]=1.Cl.[C:23]1([Mg]Br)[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1>O1CCOCC1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd]>[CH3:21][O:20][C:17]1[CH:18]=[CH:19][C:14]([C:7]2[N:8]([CH2:11][CH2:12][CH3:13])[N:9]=[C:10]3[C:6]=2[CH:5]=[CH:4][CH:3]=[C:2]3[C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)=[CH:15][CH:16]=1
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참가 물질

6

반응물 3

HCID 313Hydrochloric Acid2회HCID 688824767-chloro-3-(4-methoxyphenyl)-2-propyl-2H-indazoleHCID 178418255HCID 178418255, 화합물

생성물 1

HCID 688851453-(4-methoxyphenyl)-7-phenyl-2-propyl-2H-indazole수율 78.8%

시약·촉매·용매 2

HCID 9811564Bis(dibenzylideneacetone)palladium촉매
HCID 31275
1,4-Dioxane
용매

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온도
80 °C

실험 절차

To a stirred solution of 7-Chloro-3-(4-methoxyphenyl)-2-propyl-2H-indazole (0.200 g, 0.66 mmol) in anhydrous dioxane (6 mL) was added tris(dibenzylideneacetone)-dipalladium(0) (0.0128 g, 0.013 mmol) and 1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene.HCl (0.011 g, 0.07 mmol). Phenylmagnesium bromide (0.4 mL, 1.20 mmol, 3M in diethyl ether) was added and the reaction heated to 80° C. for 3 hours. After this time an additional equivalent of reagents was added and the reaction heated for an additional 18 hours. The reaction mixture was treated with 1N aqueous hydrochloric acid solution and extracted with ethyl acetate. The organic layer washed with water and saturated aqueous sodium chloride solution. After drying over anhydrous magnesium sulfate, the organic phase was filtered and the filtrate evaporated in vacuo to yield crude title compound. The oil was purified by silica gel column chromatography eluting with hexane/ethyl acetate (5/1) to provide the title compound as a white solid (0.178 g, 0.52 mmol, 78%).

후처리

  1. additionAfter this time an additional equivalent of reagents was added
  2. temperaturethe reaction heated for an additional 18 hours
  3. extractionextracted with ethyl acetate
  4. washThe organic layer washed with water and saturated aqueous sodium chloride solution
  5. dry with materialAfter drying over anhydrous magnesium sulfate
  6. filtrationthe organic phase was filtered
  7. customthe filtrate evaporated in vacuo
  8. customto yield crude title compound
  9. customThe oil was purified by silica gel column chromatography
  10. washeluting with hexane/ethyl acetate (5/1)

출처 및 근거

ORD 기록
ord-93eb66b16f0a427d879199118c6cdf07
출처 데이터셋
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07241791B2

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