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

HRID 64058
ノート
印刷プレビュー

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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

HCID 807IodineHCID 65185Metaperiodic acidHCID 778873-Nitropyridin-2-ylamine

生成物 1

HCID 33844682-Amino-5-iodo-3-nitropyridine収率 57%

試薬・触媒・溶媒 3

HCID 176Acetic Acid溶媒HCID 962Water溶媒
HCID 1118
Sulfuric Acid
溶媒

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
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09447091B2

反応ノート

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