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

HRID 341468
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HRID 341468 반응식
[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]
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6

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HCID 679Dimethyl SulfoxideHCID 69675Benzenamine, N,3-dimethyl-HCID 81531DiisopropylethylamineHCID 867105172-Amino-4-chloro-6-cyano-[1,3,5]triazine2회

생성물 1

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

시약·촉매·용매 1

HCID 8857
Ethyl Acetate
용매

실험 절차

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%).

후처리

  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

출처 및 근거

ORD 기록
ord-a4ad9bd160634c66bbeb68c7ef26c5cc
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08895733B2

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