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Phosphorus trichloride → 6-Amino-4-chloro-2-methylnicotinonitrile

HRID 928411
ノート
印刷プレビュー

反応式

HRID 928411 の反応式
[NH2:1][C:2]1[N:7]=[C:6]([CH3:8])[C:5]([C:9]#[N:10])=[C:4]([O-])[CH:3]=1.[Na+].P(Cl)(Cl)[Cl:14].O=P(Cl)(Cl)Cl>[OH-].[Na+]>[NH2:1][C:2]1[CH:3]=[C:4]([Cl:14])[C:5]([C:9]#[N:10])=[C:6]([CH3:8])[N:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 24387Phosphorus trichlorideHCID 24813Phosphorus oxychlorideHCID 58081220Sodium 6-amino-3-cyano-2-methylpyridin-4-olate

生成物 1

HCID 672084926-Amino-4-chloro-2-methylnicotinonitrile

試薬・触媒・溶媒 1

HCID 14798Sodium Hydroxide溶媒

実験手順

A suspension of sodium 6-amino-3-cyano-2-methylpyridin-4-olate (690 mg, 4.03 mmol, prepared in analogy to WO2001062233A2 and isolated as sodium salt) in PCl3 (3.50 ml, 40.3 mmol) and POCl3 (0.94 ml, 10.1 mmol) was heated to reflux for 12 h. After cooling to room temperature, the reaction mixture was carefully given onto 2N NaOH (200 ml) and 50 g ice. The mixture was extracted with DCM (7×50 ml), and the combined organic extracts were dried over Na2SO4, filtered and concentrated. The crude product was used without additional purification. LCMS RtM=1.45 min, [M+H]+=168.1.

後処理

  1. temperaturewas heated
  2. temperatureto reflux for 12 h
  3. extractionThe mixture was extracted with DCM (7×50 ml)
  4. dry with materialthe combined organic extracts were dried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe crude product was used without additional purification
  8. customLCMS RtM=1.45 min, [M+H]+=168.1

出典と根拠

ORDレコード
ord-87ecdb351084450eac2bdc40a97eff85
出典データセット
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09290485B2

反応ノート

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