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

HRID 2068696
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HRID 2068696 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 14797Potassium HydroxideHCID 211885311-Boc-3-bromomethylpiperidineHCID 178515446HCID 178515446, 화합물

생성물 1

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

시약·촉매·용매 1

HCID 679
Dimethyl Sulfoxide
용매

실험 절차

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)+.

후처리

  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)

출처 및 근거

ORD 기록
ord-8aae24412ae143088d3032618860ce99
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08299065B2

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