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Dimethyl Sulfoxide → 4-Cyano-N-methyl-N-3-methylphenyl-[1,3,5]triazine-2,6-diamine

HRID 341468
ノート
印刷プレビュー

反応式

HRID 341468 の反応式
[NH2:1][C:2]1[N:7]=[C:6](Cl)[N:5]=[C:4]([C:9]#[N:10])[N:3]=1.CS(C)=O.C(N(C(C)C)CC)(C)C.[CH3:24][NH:25][C:26]1[CH:31]=[CH:30][CH:29]=[C:28]([CH3:32])[CH:27]=1>C(OCC)(=O)C>[C:9]([C:4]1[N:3]=[C:2]([NH2:1])[N:7]=[C:6]([N:25]([CH3:24])[C:26]2[CH:31]=[CH:30][CH:29]=[C:28]([CH3:32])[CH:27]=2)[N:5]=1)#[N:10]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 679Dimethyl SulfoxideHCID 69675Benzenamine, N,3-dimethyl-HCID 81531DiisopropylethylamineHCID 867105172-Amino-4-chloro-6-cyano-[1,3,5]triazine2 回

生成物 1

HCID 668028104-Cyano-N-methyl-N-3-methylphenyl-[1,3,5]triazine-2,6-diamine

試薬・触媒・溶媒 1

HCID 8857
Ethyl Acetate
溶媒

実験手順

To 2-amino-4-chloro-6-cyano-[1,3,5]triazine (Prepared in an analogous way to Intermediate 3, 46 mg, 296 μmol) was added 1 mL anhydrous DMSO, diisopropylethylamine (77 μL, 444 μmol) and N-methyl-m-toluidine (40 mg, 326 μmol). The mixture was heated at 90 C for 2 h, allowed to cool and diluted with 10 mL ethyl acetate. The mixture was then extracted with water (10 mL), 0.5 M HCl (3×10 mL), water (10 mL) and saturated brine (10 mL). The organic layer was dried further over anhydrous sodium sulfate and evaporated to give the desired product which was used directly without further purification or characterization (42 mg, 59%).

後処理

  1. temperatureThe mixture was heated at 90 C for 2 h
  2. temperatureto cool
  3. extractionThe mixture was then extracted with water (10 mL), 0.5 M HCl (3×10 mL), water (10 mL) and saturated brine (10 mL)
  4. dry with materialThe organic layer was dried further over anhydrous sodium sulfate
  5. customevaporated

出典と根拠

ORDレコード
ord-a4ad9bd160634c66bbeb68c7ef26c5cc
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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