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Potassium Carbonate → methyl 4-(2,5-dimethylpyrimidin-4-yl)-1-methyl-1H-pyrazole-5-carboxylate

HRID 60136
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HRID 60136 반응식
CC1(C)C(C)(C)OBO1.Br[C:11]1[CH:12]=[N:13][N:14]([CH3:20])[C:15]=1[C:16]([O:18][CH3:19])=[O:17].C(=O)([O-])[O-].[K+].[K+].Cl[C:28]1[C:33]([CH3:34])=[CH:32][N:31]=[C:30]([CH3:35])[N:29]=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.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd].C1(P(C2CCCCC2)C2C=CC=CC=2C2C(OC)=CC=CC=2OC)CCCCC1.O.O1CCOCC1.C(N(CC)CC)C>[CH3:35][C:30]1[N:31]=[C:32]([C:11]2[CH:12]=[N:13][N:14]([CH3:20])[C:15]=2[C:16]([O:18][CH3:19])=[O:17])[C:33]([CH3:34])=[CH:28][N:29]=1
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참가 물질

10

반응물 4

HCID 11430Potassium CarbonateHCID 673643Methyl 4-bromo-1-methyl-1H-pyrazole-5-carboxylateHCID 27347684,4,5,5-Tetramethyl[1,3,2]dioxaborolane2회HCID 124653814-Chloro-2,5-dimethylpyrimidine

생성물 1

HCID 90383435methyl 4-(2,5-dimethylpyrimidin-4-yl)-1-methyl-1H-pyrazole-5-carboxylate수율 110%

시약·촉매·용매 5

HCID 9811564Bis(dibenzylideneacetone)palladium촉매
HCID 112698722-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl촉매
HCID 962Water용매
HCID 8471Triethylamine용매
HCID 312751,4-Dioxane용매2회

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온도
100 °C

실험 절차

4,4,5,5-Tetramethyl-1,3,2-dioxaborolane (1.5 ml) was added to a 1,4-dioxane (19 ml) solution of methyl 4-bromo-1-methyl-1H-pyrazole-5-carboxylate (1.9 g), 2-dicyclohexylphosphino-2′,6′-dimethoxy-1,1′-biphenyl (0.15 g), Tris(dibenzylideneacetone)dipalladium(0) (0.16 g), and triethylamine (3.7 ml). The obtained mixture was stirred in a nitrogen atmosphere at 100° C. for 30 minutes. Thereafter, 4,4,5,5-tetramethyl-1,3,2-dioxaborolane (1.5 ml) was added to the reaction solution, and the obtained mixture was then stirred for 30 minutes at the same temperature as described above. Thereafter, an aqueous solution (3.9 ml) of potassium carbonate (3.6 g) and a 1,4-dioxane (4 ml) solution of 4-chloro-2,5-dimethylpyrimidine (1.0 g) were successively added to the reaction solution, and the obtained mixture was then stirred at the same temperature as described above for 1 hour. Thereafter, water was added to the reaction solution, and the mixed solution was extracted with ethyl acetate and was then dried over anhydrous sodium sulfate. The solvent was distilled away under reduced pressure, and the obtained residue was purified by silica gel column chromatography (silica gel:eluent; heptane:ethyl acetate=3:1-1:1-0:1), so as to obtain the title compound (1.9 g) in the form of an orange liquid.

후처리

  1. stirringthe obtained mixture was then stirred for 30 minutes at the same temperature
  2. stirringthe obtained mixture was then stirred at the same temperature
  3. customas described above for 1 hour
  4. extractionthe mixed solution was extracted with ethyl acetate
  5. dry with materialwas then dried over anhydrous sodium sulfate
  6. distillationThe solvent was distilled away under reduced pressure
  7. customthe obtained residue was purified by silica gel column chromatography (silica gel:eluent; heptane:ethyl acetate=3:1-1:1-0:1)

출처 및 근거

ORD 기록
ord-703c64c185294d3fb38394e58541bf0b
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09440970B2

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