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Phosphorus oxychloride → 6-bromo-2-chloro-N-methyl-4-nitropyridin-3-amine

HRID 2209025
ノート
印刷プレビュー

反応式

HRID 2209025 の反応式
[Br:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[C:5]([NH:11][CH3:12])=[CH:4][N+:3]=1[O-].P(Cl)(Cl)([Cl:16])=O>>[Br:1][C:2]1[N:3]=[C:4]([Cl:16])[C:5]([NH:11][CH3:12])=[C:6]([N+:8]([O-:10])=[O:9])[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

3

反応物 2

HCID 24813Phosphorus oxychlorideHCID 866591292-Bromo-5-(methylamino)-4-nitropyridine 1-oxide

生成物 1

HCID 1178440196-bromo-2-chloro-N-methyl-4-nitropyridin-3-amine

反応条件

温度
110 °C

実験手順

A suspension of 2-bromo-5-(methylamino)-4-nitropyridine 1-oxide (3.35 g, 13.51 mmol) in phosphorous oxychloride (35 mL, 374 mmol) was heated at 110° C. After 1 h, the reaction mixture was cooled to r.t. and evaporated to dryness in vacuo. The residue was partitioned between EtOAc (100 mL) and saturated sodium hydrogen carbonate, the layers were separated and the organic layer was washed with brine and dried over MgSO4. The residue was purified by flash column chromatography (SiO2, 0% EtOAc/Hexanes to 30% EtOAc/hexanes) to give 6-bromo-2-chloro-N-methyl-4-nitropyridin-3-amine 2.59.

後処理

  1. temperaturethe reaction mixture was cooled to r.t.
  2. customevaporated to dryness in vacuo
  3. customThe residue was partitioned between EtOAc (100 mL) and saturated sodium hydrogen carbonate
  4. customthe layers were separated
  5. washthe organic layer was washed with brine
  6. dry with materialdried over MgSO4
  7. customThe residue was purified by flash column chromatography (SiO2, 0% EtOAc/Hexanes to 30% EtOAc/hexanes)

出典と根拠

ORDレコード
ord-f27ea1e480114069932cd0c688d4a9f6
出典データセット
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09376441B2

反応ノート

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