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Potassium Carbonate → 3-[5-(2-Fluoro-3-methoxy-phenyl)-pyridin-2-yloxy]-azetidine-1-carboxylic acid pyridazin-3-ylamide

HRID 2097598
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HRID 2097598 반응식
[F:1][C:2]1[C:7]([O:8][CH3:9])=[CH:6][CH:5]=[CH:4][C:3]=1B(O)O.[N:13]1[CH:18]=[CH:17][CH:16]=[C:15]([NH:19][C:20]([N:22]2[CH2:25][CH:24]([O:26][C:27]3[CH:32]=[CH:31][C:30](Br)=[CH:29][N:28]=3)[CH2:23]2)=[O:21])[N:14]=1.C(=O)([O-])[O-].[K+].[K+]>C1COCC1.O.C(OCC)(=O)C>[N:13]1[CH:18]=[CH:17][CH:16]=[C:15]([NH:19][C:20]([N:22]2[CH2:23][CH:24]([O:26][C:27]3[CH:32]=[CH:31][C:30]([C:3]4[CH:4]=[CH:5][CH:6]=[C:7]([O:8][CH3:9])[C:2]=4[F:1])=[CH:29][N:28]=3)[CH2:25]2)=[O:21])[N:14]=1
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참가 물질

6

반응물 3

HCID 11430Potassium CarbonateHCID 49857442-Fluoro-3-methoxyphenylboronic acidHCID 667103553-(5-Bromo-pyridin-2-yloxy)-azetidine-1-carboxylic acid pyridazin-3-ylamide

생성물 1

HCID 442189013-[5-(2-Fluoro-3-methoxy-phenyl)-pyridin-2-yloxy]-azetidine-1-carboxylic acid pyridazin-3-ylamide수율 79.9%

시약·촉매·용매 2

HCID 8857
Ethyl Acetate
용매
HCID 21881883Oxolane--water (1/1)용매

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온도
100 °C

실험 절차

A solution of 2-fluoro-3-methoxyphenyl boronic acid (0.065 g, 0.38 mmol) in THF/H2O (10:1; 2 mL) was added to a microwave vial containing 3-(5-bromo-pyridin-2-yloxy)-azetidine-1-carboxylic acid pyridazin-3-ylamide (prepared in Step 1) (0.100 g, 0.25 mmol) and potassium carbonate (0.105 g, 0.76 mmol). Nitrogen gas was bubbled through the mixture for 5 mins then 1,1′-bis[(diphenylphosphino)-ferrocene]dichloropalladium(II) complex with CH2Cl2 (0.020 g, 10 mole %) was added and the vial sealed and heated at 100° C. in microwave synthesiser for 30 min. The cooled reaction mixture was diluted with ethyl acetate (20 mL) and washed sequentially with sat. aqueous sodium carbonate solution (20 mL) then sat. sodium chloride solution (20 mL). Mixture dried over magnesium sulphate and filtered. Filtrate solvents were removed in vacuo to afford a brown gum, which was purified by flash chromatography, eluting with a gradient of 80 to 100% ethyl acetate in hexane to a afford an off-white solid (0.079 g, 78%).

후처리

  1. customNitrogen gas was bubbled through the mixture for 5 mins
  2. addition1,1′-bis[(diphenylphosphino)-ferrocene]dichloropalladium(II) complex with CH2Cl2 (0.020 g, 10 mole %) was added
  3. customthe vial sealed
  4. customThe cooled reaction mixture
  5. washwashed sequentially with sat. aqueous sodium carbonate solution (20 mL)
  6. dry with materialMixture dried over magnesium sulphate
  7. filtrationfiltered
  8. customFiltrate solvents were removed in vacuo
  9. customto afford a brown gum, which
  10. customwas purified by flash chromatography
  11. washeluting with a gradient of 80 to 100% ethyl acetate in hexane to

출처 및 근거

ORD 기록
ord-cc55f647572248a99d275f1842cd30cb
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08450346B2

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