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Sodium Carbonate → 4-[5-(4-Methanesulfonylphenyl)-2,3-dihydrobenzofuran-2-yl]piperidine

HRID 1622224
ノート
印刷プレビュー

反応式

HRID 1622224 の反応式
Br[C:2]1[CH:3]=[CH:4][C:5]2[O:9][CH:8]([CH:10]3[CH2:15][CH2:14][N:13](C(=O)C(F)(F)F)[CH2:12][CH2:11]3)[CH2:7][C:6]=2[CH:22]=1.[CH3:23][S:24]([C:27]1[CH:32]=[CH:31][C:30](B(O)O)=[CH:29][CH:28]=1)(=[O:26])=[O:25].C([O-])([O-])=O.[Na+].[Na+]>CN(C)C=O>[CH3:23][S:24]([C:27]1[CH:32]=[CH:31][C:30]([C:2]2[CH:3]=[CH:4][C:5]3[O:9][CH:8]([CH:10]4[CH2:11][CH2:12][NH:13][CH2:14][CH2:15]4)[CH2:7][C:6]=3[CH:22]=2)=[CH:29][CH:28]=1)(=[O:26])=[O:25]
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

5

反応物 3

HCID 10340Sodium CarbonateHCID 27343644-(Methanesulfonyl)phenylboronic acidHCID 866748871-[4-(5-Bromo-2,3-dihydro-benzofuran-2-yl)-piperidin-1-yl]-2,2,2-trifluoro-ethanone

生成物 1

HCID 679732894-[5-(4-Methanesulfonylphenyl)-2,3-dihydrobenzofuran-2-yl]piperidine

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
90 °C

実験手順

To a mixture of 1-[4-(5-bromo-2,3-dihydro-benzofuran-2-yl)-piperidin-1-yl]-2,2,2-trifluoro-ethanone (2.50 g) and 4-(methanesulfonyl)phenyl boronic acid (1.45 g) in N,N-dimethylformamide (25 mL) a 2 M aqueous Na2CO3 solution (8.26 mL) is added. The mixture is sparged with argon for 10 min and PdCl2[1,1′-bis(diphenylphosphino)-ferrocene].CH2Cl2 complex (540 mg) is added. The resulting mixture is stirred over night at 90° C. After cooling to room temperature, water (50 mL) and ethyl acetate (100 mL) are added and the aqueous phase is extracted with ethyl acetate. The organic phase is washed with water and brine, dried (MgSO4), and the solvent is evaporated. The residue is chromatographed on silica gel [dichloromethane/(methanol/NH4OH 9:1) 90:10-80:20] to give the title compound, since the trifluoroacetyl group is removed under the reaction conditions. LC (method 1): tR=0.88 min; Mass spectrum (ESI+): m/z=358 [M+H]+.

後処理

  1. additionis added
  2. customThe mixture is sparged with argon for 10 min
  3. additionCH2Cl2 complex (540 mg) is added
  4. temperatureAfter cooling to room temperature
  5. additionwater (50 mL) and ethyl acetate (100 mL) are added
  6. extractionthe aqueous phase is extracted with ethyl acetate
  7. washThe organic phase is washed with water and brine
  8. dry with materialdried (MgSO4)
  9. customthe solvent is evaporated
  10. customThe residue is chromatographed on silica gel [dichloromethane/(methanol/NH4OH 9:1) 90:10-80:20]

出典と根拠

ORDレコード
ord-af40e06ca50547488d98f42f0d442ab4
出典データセット
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08778926B2

反応ノート

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