Water → HCID 18427783, compound

HRID 1871622Notes

Reaction equation

HRID 1871622 reaction equation
[CH3:1][S:2][C:3](SC)=[C:4]([S:7]([C:10]1[CH:15]=[CH:14][CH:13]=[C:12]([C:16]([F:19])([F:18])[F:17])[CH:11]=1)(=[O:9])=[O:8])[C:5]#[N:6].[Cl:22][C:23]1[CH:28]=[C:27]([C:29]([F:32])([F:31])[F:30])[CH:26]=[C:25]([Cl:33])[C:24]=1[NH:34][NH2:35].O>C(O)C>[NH2:6][C:5]1[N:34]([C:24]2[C:23]([Cl:22])=[CH:28][C:27]([C:29]([F:30])([F:32])[F:31])=[CH:26][C:25]=2[Cl:33])[N:35]=[C:3]([S:2][CH3:1])[C:4]=1[S:7]([C:10]1[CH:15]=[CH:14][CH:13]=[C:12]([C:16]([F:18])([F:19])[F:17])[CH:11]=1)(=[O:9])=[O:8]

Participants

5

Procedure

A suspension of 0.50 g (1.42 mmol) of 3,3-bis-methylthio-2-(3-trifluoromethylphenylsulfonyl) acrylonitrile and 0.35 g (1.42 mmol) of 2,6-dichloro4-trifluoromethylphenylhydrazine in 10 mL of ethanol was heated at reflux for 2.5 hours, solution occurring as the reaction mixture was warmed. The mixture was stirred overnight at room temperature and was then poured into cold water. The product was extracted into ethyl acetate and the extracts were dried with magnesium sulfate and evaporated. The residues were crystallized from ether, and the product was filtered off and air dried to give 314 mg (40%) of the desired product, m.p. 201-203° C. Anal. Calcd. for C18H11O2N3S2Cl2F6 : C, 39.28; H, 2.02; N, 7.64. Found: C, 39.35; H, 2.19; N, 7.48.

Workup

  1. temperaturewas heated
  2. temperatureat reflux for 2.5 hours
  3. temperaturewas warmed
  4. extractionThe product was extracted into ethyl acetate
  5. dry with materialthe extracts were dried with magnesium sulfate
  6. customevaporated
  7. customThe residues were crystallized from ether
  8. filtrationthe product was filtered off
  9. customair dried

Sources & evidence

ORD record
ord-fb4ce86382514fe5b663fa6175528cda
Source dataset
uspto-grants-2000_08
Patent number
US06103900

Reaction notes

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