Methanol → 1-(2-[4-(2-[2,2,2-Trifluoroethyl]guanidino)pyrimid-2-yl-methylthio]ethylamino)-2-methylaminocyclobutene-3,4-dione

HRID 1902297

Reaktionsgleichung

Reaktionsgleichung von HRID 1902297
[F:1][C:2]([F:20])([F:19])[CH2:3][N:4]=[C:5]([NH2:18])[NH:6][C:7]1[CH:12]=[CH:11][N:10]=[C:9]([CH2:13][S:14][CH2:15][CH2:16][NH2:17])[N:8]=1.CO.C[O:24][C:25]1[C:28](=O)[C:27](=O)[C:26]=1[O:31]C.[CH3:33][NH2:34]>C(O)C>[F:20][C:2]([F:1])([F:19])[CH2:3][N:4]=[C:5]([NH2:18])[NH:6][C:7]1[CH:12]=[CH:11][N:10]=[C:9]([CH2:13][S:14][CH2:15][CH2:16][NH:17][C:28]2[C:25](=[O:24])[C:26](=[O:31])[C:27]=2[NH:34][CH3:33])[N:8]=1

Komponenten

6

Versuchsvorschrift

A mixture of 4-[2-(2,2,2-trifluoroethyl)-guanidino]-2-(2-aminoethyl)thiomethylpyrimidine (0.31 g.), methanol (5 ml.) and 1,2-dimethoxycyclobutene-3,4-dione (0.14 g.) was stirred at room temperature for 18 hours. A 33% w/v solution of methylamine in ethanol (5 ml.) was added and the mixture left at room temperature for 18 hours and then evaporated to dryness. The residue was purified by preparative thin layer chromatography using ethyl acetate/methanol/ammonia 6:1:0.5 v/v/v as developing solvent to give 1-(2-[4-(2-[2,2,2-trifluoroethyl]guanidino)pyrimid-2-yl-methylthio]ethylamino)-2-methylaminocyclobutene-3,4-dione (0.16 g.) characterised as the hydrogen maleate, m.p. 178°-184° after recrystallisation from a mixture of methanol and acetonitrile.

Aufarbeitung

  1. additionwas added
  2. waitthe mixture left at room temperature for 18 hours
  3. customevaporated to dryness
  4. customThe residue was purified by preparative thin layer chromatography

Quellen und Nachweise

ORD-Eintrag
ord-051a4ff556b544299b96e14bb8f885ab
Quelldatensatz
uspto-grants-1982_12
Patentnummer
US04362728

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