Tetrahydrofuran → N-(3-Amino-4-thienyl)-N'-(2,6-dichlorophenyl)thiourea

HRID 349413

反応式

HRID 349413 の反応式
Cl.Cl.[NH2:3][C:4]1[C:8]([NH2:9])=[CH:7][S:6][CH:5]=1.C1COCC1.C(N(C(C)C)C(C)C)C.[Cl:24][C:25]1[CH:30]=[CH:29][CH:28]=[C:27]([Cl:31])[C:26]=1[N:32]=[C:33]=[S:34]>C(OCC)(=O)C>[NH2:3][C:4]1[C:8]([NH:9][C:33]([NH:32][C:26]2[C:27]([Cl:31])=[CH:28][CH:29]=[CH:30][C:25]=2[Cl:24])=[S:34])=[CH:7][S:6][CH:5]=1

参加物

6

実験手順

A mixture of 1.87 g of 3,4-diaminothiophene dihydrochloride, 60 ml of anhydrous THF and 2.58 g of N-ethyl-N,N-diisopropylamine was stirred at room temperature for 30 minutes and then admixed with 2.04 g of 2,6-dichlorophenyl isothiocyanate. After the mixture had been heated to 40° C. for 10 minutes, it was stirred at room temperature for approx. 18 hours, and the solvent was distilled off, and the residue admixed with water and extracted repeatedly with ethyl acetate. After the combined organic phases had been treated with activated carbon, they were dried over sodium sulfate and the solvent was again distilled off. A crystalline solid was obtained and, after stirring with a little ethyl acetate, was filtered off. M.p. 165° C.

後処理

  1. temperatureAfter the mixture had been heated to 40° C. for 10 minutes
  2. stirringit was stirred at room temperature for approx. 18 hours
  3. distillationthe solvent was distilled off
  4. extractionthe residue admixed with water and extracted repeatedly with ethyl acetate
  5. additionAfter the combined organic phases had been treated with activated carbon, they
  6. dry with materialwere dried over sodium sulfate
  7. distillationthe solvent was again distilled off
  8. customA crystalline solid was obtained
  9. filtrationwas filtered off

出典と根拠

ORDレコード
ord-241168cd9bac4a46b0fa26436f3bd4f8
出典データセット
uspto-grants-2007_02
特許番号
US07179830B2

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