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Water → tert-Butyl 3-[(4-bromo-2-oxopyridin-1(2H)-yl)methyl]piperidine-1-carboxylate

HRID 2068696
ノート
印刷プレビュー

反応式

HRID 2068696 の反応式
[OH:1][C:2]1[CH:7]=[C:6]([Br:8])[CH:5]=[CH:4][N:3]=1.[OH-].[K+].[C:11]([N:18]1[CH2:23][CH2:22][CH2:21][CH:20]([CH2:24]Br)[CH2:19]1)([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12].O>CS(C)=O>[Br:8][C:6]1[CH:5]=[CH:4][N:3]([CH2:24][CH:20]2[CH2:21][CH2:22][CH2:23][N:18]([C:11]([O:13][C:14]([CH3:15])([CH3:17])[CH3:16])=[O:12])[CH2:19]2)[C:2](=[O:1])[CH:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 14797Potassium HydroxideHCID 211885311-Boc-3-bromomethylpiperidineHCID 178515446HCID 178515446、化合物

生成物 1

HCID 68733845tert-Butyl 3-[(4-bromo-2-oxopyridin-1(2H)-yl)methyl]piperidine-1-carboxylate収率 95%

試薬・触媒・溶媒 1

HCID 679
Dimethyl Sulfoxide
溶媒

実験手順

To a solution of 2-hydroxy-4-bromopyridine (0.10 g, 0.57 mmol) in DMSO (1.50 mL) was added KOH (0.095 g, 1.70 mmol) and the resulting reaction mixture was stirred for 10 min at room temperature followed by addition of 1-Boc-3-bromomethylpiperidine (0.16 g, 0.57 mmol). The reaction mixture was then stirred at 45° C. for 16 h. After the completion of reaction (TLC monitoring), water was added to the reaction and extracted with EtOAc (3×25 mL). The combined organics was washed with brine, dried (Na2SO4), filtered and concentrated. The residue was purified over silica gel (100-200 M, 1% MeOH-DCM) to obtain the desired product (0.15 g, 95%). MS: 371.10 (M+H)+.

後処理

  1. customthe resulting reaction mixture
  2. stirringThe reaction mixture was then stirred at 45° C. for 16 h
  3. additionwas added to the reaction
  4. extractionextracted with EtOAc (3×25 mL)
  5. washThe combined organics was washed with brine
  6. dry with materialdried (Na2SO4)
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customThe residue was purified over silica gel (100-200 M, 1% MeOH-DCM)

出典と根拠

ORDレコード
ord-8aae24412ae143088d3032618860ce99
出典データセット
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08299065B2

反応ノート

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