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

HRID 1469382
ノート
印刷プレビュー

反応式

HRID 1469382 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 2

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

反応条件

温度
100 °C

実験手順

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%).

後処理

  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

出典と根拠

ORDレコード
ord-f18a26a026884b47a8d3b31c4a64be7c
出典データセット
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09006269B2

反応ノート

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