Potassium Hydroxide → HCID 178456993, Verbindung

HRID 1975929Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1975929
[OH-].[K+].Cl[C:4]1[S:12][C:11]2[S:10](=[O:14])(=[O:13])[N:9]=[C:8]([NH:15][CH:16]([CH3:18])[CH3:17])[NH:7][C:6]=2[CH:5]=1>CO.[Pd]>[CH:16]([NH:15][C:8]1[NH:7][C:6]2[CH:5]=[CH:4][S:12][C:11]=2[S:10](=[O:13])(=[O:14])[N:9]=1)([CH3:18])[CH3:17]

Komponenten

5

Versuchsvorschrift

Powdered potassium hydroxide (128 mg, 2.28 mmol) was added to a solution of 6-chloro-3-isopropylamino-4H-thieno[3,2-e]-1,2,4-thiadiazine 1,1-dioxide (319 mg, 1.14 mmol) in 25 ml of methanol and the mixture was hydrogenated at room temperature and atmospheric pressure for 3 days with 150 mg of 10% palladium on carbon. The catalyst was removed by filtration and washed with ethanol and water. The combined filtrate was acidified with 4 M hydrochloric acid and evaporated to dryness. The residue was recrystallised from water/ethanol and finally from ethyl acetate with decolorising charcoal affording the title compound contaminated with starting material, which could be removed by silica gel column chromatography; 1H-NMR (DMSO-d6): δ1.16 (d, 6H, 2×CH3), 3.88 (m, 1H, CH), 6.95 (d, 1H, H-5), 7.03 (br d, 1H, NH), 7.88 (d, 1H, H-6), 10.70 (br s, 1H).

Aufarbeitung

  1. customwas hydrogenated at room temperature
  2. customThe catalyst was removed by filtration
  3. washwashed with ethanol and water
  4. customevaporated to dryness
  5. customThe residue was recrystallised from water/ethanol and finally from ethyl acetate with decolorising charcoal affording the title compound
  6. customcould be removed by silica gel column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-cbf5d864f47b4ffdac1d29e8061750fe
Quelldatensatz
uspto-grants-2001_05
Patentnummer
US06225310B1

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