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Hydrochloric Acid → N-methoxy-N-methyl-2-oxopiperidine-4-carboxamide

HRID 535314
ノート
印刷プレビュー

反応式

HRID 535314 の反応式
[O:1]=[C:2]1[CH2:7][CH:6]([C:8]([OH:10])=O)[CH2:5][CH2:4][NH:3]1.C1N=CN(C(N2C=NC=C2)=O)C=1.[CH3:23][NH:24][O:25][CH3:26].Cl.O1CCOCC1>C(Cl)Cl>[CH3:26][O:25][N:24]([CH3:23])[C:8]([CH:6]1[CH2:5][CH2:4][NH:3][C:2](=[O:1])[CH2:7]1)=[O:10]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 313Hydrochloric AcidHCID 14232N,O-DimethylhydroxylamineHCID 312751,4-DioxaneHCID 682631,1'-CarbonyldiimidazoleHCID 552860802-Oxopiperidine-4-carboxylic acid

生成物 1

HCID 86718437N-methoxy-N-methyl-2-oxopiperidine-4-carboxamide

試薬・触媒・溶媒 1

HCID 6344
Dichloromethane
溶媒

実験手順

To a stirred solution of 2-oxopiperidine-4-carboxylic acid (CAS #24537-50-6) (1.4 g, 9.78 mmol) in DCM (20 ml) was added portion wise CDI (1.665 g, 10.27 mmol). The suspension was stirred at room temperature for 5 hrs and N,O-dimethylhydroxylamine (1.002 g, 10.27 mmol) was added to the suspension and the reaction mixture was stirred overnight at room temperature. HCl (4M) in 1,4-dioxane (2.445 ml, 9.78 mmol) was added to the cloudy brown-orange solution and the reaction was stirred for 30 min (pH 7). The white precipitate was filtered off and the filtrate was washed with aqueous NaHCO3 solution. The organic phase was dried over Na2SO4, filtered and concentrated in vacuo to obtain the title compound as brown liquid.

後処理

  1. stirringthe reaction mixture was stirred overnight at room temperature
  2. stirringthe reaction was stirred for 30 min (pH 7)
  3. filtrationThe white precipitate was filtered off
  4. washthe filtrate was washed with aqueous NaHCO3 solution
  5. dry with materialThe organic phase was dried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-e91d84a9492f45df90da9a2496b8bc82
出典データセット
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08859535B2

反応ノート

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