Iodine → 2-Amino-5-iodo-3-nitropyridine

HRID 64058

反応式

HRID 64058 の反応式
[N+:1]([C:4]1[C:5]([NH2:10])=[N:6][CH:7]=[CH:8][CH:9]=1)([O-:3])=[O:2].[I:11](O)(=O)(=O)=O.II>C(O)(=O)C.O.S(=O)(=O)(O)O>[I:11][C:8]1[CH:9]=[C:4]([N+:1]([O-:3])=[O:2])[C:5]([NH2:10])=[N:6][CH:7]=1

参加物

7

反応条件

温度
90 °C

実験手順

To a solution of 3-nitropyridin-2-amine (1.2 g, 8.63 mmol) in acetic acid (5 ml), water (1 ml) and sulfuric acid (0.2 ml) was added periodic acid (0.4 g, 1.72 mmol, 0.2 eq.) and the mixture was stirred at 90° C. for 15 min. Iodine (0.87 g, 3.45 mmol, 0.4 eq.) was added portionwise and the mixture was heated at 90° C. for 1 h. The mixture was quenched by the addition of water and extracted with ethylacetate (3×150 ml). The combined organic layer was washed with water, aqueous sodium thiosulfate, brine and dried over sodium sulphate. The solvent was distilled off to give the product in 57% yield (1.3 g). 1H NMR (300 MHz, DMSO-d6): δ 8.58 (d, 1H), 8.54 (d, 1H) 8.04 (br s, 2H); LC-MS (ESI); Calculated mass: 265.01: Observed mass: 265.9 [M+H]+ (rt: 1.36 min).

後処理

  1. temperaturethe mixture was heated at 90° C. for 1 h
  2. customThe mixture was quenched by the addition of water
  3. extractionextracted with ethylacetate (3×150 ml)
  4. washThe combined organic layer was washed with water, aqueous sodium thiosulfate, brine
  5. dry with materialdried over sodium sulphate
  6. distillationThe solvent was distilled off
  7. customto give the product in 57% yield (1.3 g)
  8. custom265.9 [M+H]+ (rt: 1.36 min)

出典と根拠

ORDレコード
ord-f38c30b13fc04fbdbd1db143828f51c7
出典データセット
uspto-grants-2016_09
特許番号
US09447091B2

関連ノート

読み込み中…