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Sodium Carbonate → 2-Amino-4-chloro-6-cyano-[1,3,5]triazine

HRID 341467
ノート
印刷プレビュー

反応式

HRID 341467 の反応式
[NH2:1][C:2]1[NH:3][C:4](=O)[N:5]=[C:6]([C:8]#[N:9])[N:7]=1.P(Cl)(Cl)([Cl:13])=O.C(=O)([O-])[O-].[Na+].[Na+]>>[NH2:1][C:2]1[N:3]=[C:4]([Cl:13])[N:5]=[C:6]([C:8]#[N:9])[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

4

反応物 3

HCID 10340Sodium CarbonateHCID 24813Phosphorus oxychlorideHCID 178510604HCID 178510604、化合物

生成物 1

HCID 867105172-Amino-4-chloro-6-cyano-[1,3,5]triazine

実験手順

To 2-amino-4-cyano-6-oxo-1,3,5-triazine (J. Am. Chem. Soc., 1961, 83, 1261-2, 2.30 g, 16.8 mmol) was added phosphoryl trichloride (50 mL, 547 mmol) and the mixture heated at 90 C for 2 h. The reaction mixture was cooled to room temperature before pouring onto ice-water (250 mL) and basifying to pH 8 with solid sodium carbonate. The mixture was then extracted into DCM (3×250 mL) and the combined organics were dried over anhydrous sodium sulfate and concentrated under reduced pressure to afford the desired compound, which was used crude without further purification (343 mg, 13%). Method C HPLC-MS: 2 MH+ requires m/z=311. Found: m/z=311, Rt=0.74 min (100%).

後処理

  1. temperaturethe mixture heated at 90 C for 2 h
  2. additionbefore pouring onto ice-water (250 mL)
  3. extractionThe mixture was then extracted into DCM (3×250 mL)
  4. dry with materialthe combined organics were dried over anhydrous sodium sulfate
  5. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-db512cb438324479b5a864c1065ab6f9
出典データセット
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08895733B2

反応ノート

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