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Dimethylformamide → 2-(4-aminopiperidin-1-yl)-N-methylacetamide

HRID 914069
ノート
印刷プレビュー

反応式

HRID 914069 の反応式
[NH:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.C([O-])([O-])=O.[K+].[K+].Cl[CH2:14][C:15]([NH:17][CH3:18])=[O:16].C[N:20](C=O)C>CCOC(C)=O>[NH2:20][CH:4]1[CH2:5][CH2:6][N:1]([CH2:14][C:15]([NH:17][CH3:18])=[O:16])[CH2:2][CH2:3]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 4

HCID 6228DimethylformamideHCID 8082PiperidineHCID 11430Potassium CarbonateHCID 667732-chloro-N-methylacetamide

生成物 1

HCID 180711782-(4-aminopiperidin-1-yl)-N-methylacetamide

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒

反応条件

温度
50 °C

実験手順

To a solution of 2.0 g (10 mmoles) of piperidine, which as dissolved in DMF, anhydrous, 100 mL, was added 2.8 g (20 mmoles) K2CO3, and 1.2 g (11 mmoles) 2-chloro-N-methylacetamide. After stirring at 50° C. for overnight, the mixture was diluted with 500 mL of EtOAc, washed with brine (3×500 mL), dried over Na2SO4, and solvent was evaporated in vacuum. The resulting residue was treated with 50% TFA/DCM and was stirred at r.t. for 2 hrs, and solvent was evaporated in vacuum. The resulting mixture was purified by prep HPLC to give yellow oil, yield 1.5 g (88%). [M+H] calc'd for C8H17N3O, 172. found 172.

後処理

  1. washwashed with brine (3×500 mL)
  2. dry with materialdried over Na2SO4, and solvent
  3. customwas evaporated in vacuum
  4. additionThe resulting residue was treated with 50% TFA/DCM
  5. stirringwas stirred at r.t. for 2 hrs
  6. customsolvent was evaporated in vacuum
  7. customThe resulting mixture was purified by prep HPLC
  8. customto give yellow oil, yield 1.5 g (88%)

出典と根拠

ORDレコード
ord-c6cd05ba0044442f8da2291f80e3f789
出典データセット
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08026234B2

反応ノート

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