2-(3-nitro-1H-pyrazol-1-yl)ethanol → 2-(3-Amino-1H-pyrazol-1-yl)ethan-1-ol

HRID 1261478ノート

反応式

HRID 1261478 の反応式
[N+:1]([C:4]1[CH:8]=[CH:7][N:6]([CH2:9][CH2:10][OH:11])[N:5]=1)([O-])=O.[H][H]>C(O)C.[Pd]>[NH2:1][C:4]1[CH:8]=[CH:7][N:6]([CH2:9][CH2:10][OH:11])[N:5]=1

参加物

5

実験手順

A solution 2-(3-nitro-pyrazol-1-yl)-ethanol (3.46 g, 22.02 mmol) in ethanol (40 mL) was placed in a Parr shaker bottle and treated with 10% palladium on carbon (350 mg). The bottle was then put on the Parr shaker and charged with hydrogen to 50 psi and let shake for 1 h. After this time, the reaction mixture was filtered through celite and the celite washed with ethanol. The filtrate was then concentrated in vacuo and azeotroped with acetonitrile and then chloroform to afford 2-(3-amino-pyrazol-1-yl)-ethanol (3.02 g, >quant.) as a light yellow viscous oil: 1H NMR (300 MHz, DMSO-d6 δ ppm 7.26 (d, J=1.83 Hz, 1H), 5.34 (d, J=2.20 Hz, 1H), 4.76 (t, J=5.31 Hz, 1H), 4.50 (s, 2H), 3.78-3.88 (m, 2H), 3.62 (q, J=5.74 Hz, 2H).

後処理

  1. filtrationAfter this time, the reaction mixture was filtered through celite
  2. washthe celite washed with ethanol
  3. concentrationThe filtrate was then concentrated in vacuo
  4. customazeotroped with acetonitrile

出典と根拠

ORDレコード
ord-2459a1673ec34672b976dd713410ab5d
出典データセット
uspto-grants-2013_06
特許番号
US08470866B2

反応ノート

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