Water → HCID 12600751, Verbindung

HRID 1078368Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1078368
[C:1]1([C:7]2[S:11][N:10]=[C:9](OCCCCl)[N:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.O>ClCCl>[C:1]1([C:7]2[S:11][N:10]=[CH:9][N:8]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1

Komponenten

4

Reaktionsbedingungen

Temperatur
65 °C

Versuchsvorschrift

0.85 g of the product obtained above were reacted with 0.7 g of 3-(5-phenyl-1,2,4-thiadiazole-3-yloxy)-propyl chloride [for preparation, see Example 54 B)] and the reaction mixture was stirred for 10.5 hours at 65° C. Then the reaction mixture was dissolved in dichloromethane and the solution shaken with water. The dichloromethane phase was separated, dried, and concentrated. The crude product obtained was purified by medium-pressure chromatography on fine-grained silica gel (Lichroprep Si 60®) using 9:1 ethyl acetate/methanol as the eluent. 0.5 g of 3-{3-[N-[2-(4-(2-trimethylsilyl)-ethoxymethoxy)-3-methoxyphenyl)-ethyl]-N-methylamino]-propyloxy)-5-phenyl-1,2,4-thiadiazole were obtained as a colorless oil.

Aufarbeitung

  1. customfor preparation
  2. customThe dichloromethane phase was separated
  3. customdried
  4. concentrationconcentrated
  5. customThe crude product obtained
  6. customwas purified by medium-pressure chromatography on fine-grained silica gel (Lichroprep Si 60®)

Quellen und Nachweise

ORD-Eintrag
ord-3b030090e8de4f59a0c1fc5116126ae5
Quelldatensatz
uspto-grants-1996_08
Patentnummer
US05547967

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