2-Chloro-6-(1-piperazinyl)pyrazine → 2-(3-Thienylmethoxy)-6-(1-Piperazinyl)Pyrazine

HRID 1296675

Reaktionsgleichung

Reaktionsgleichung von HRID 1296675
[S:1]1[CH:5]=[CH:4][C:3]([CH2:6][OH:7])=[CH:2]1.Cl[C:9]1[N:14]=[C:13]([N:15]2[CH2:20][CH2:19][NH:18][CH2:17][CH2:16]2)[CH:12]=[N:11][CH:10]=1>>[S:1]1[CH:5]=[CH:4][C:3]([CH2:6][O:7][C:9]2[CH:10]=[N:11][CH:12]=[C:13]([N:15]3[CH2:16][CH2:17][NH:18][CH2:19][CH2:20]3)[N:14]=2)=[CH:2]1

Komponenten

3

Edukt 2

HCID 1079922-Chloro-6-(1-piperazinyl)pyrazineHCID 123570Thiophene-3-methanol

Produkt 1

HCID 98786962-(3-Thienylmethoxy)-6-(1-Piperazinyl)PyrazineAusbeute 64,7 %

Reaktionsbedingungen

Temperatur
105 °C

Versuchsvorschrift

The title compound was prepared according to the procedure of Example 20 starting from 3-thiophenemethanol (6.05 g, 53.0 mmol), K-t-BuO (0.897 g, 7.99 mmol) and 6-chloro-2-(1-piperazinyl)pyrazine (0.845 g, 4.25 mmol: obtained in Example 13, step 2). The reaction mixture was stirred at 105° C. for 7.5 h. Following chromatography on silica, solvents were evaporated off. The remaining oil was redissolved in ethyl acetetate and filtered through a short plug of alumina (5×3 cm) using ether/MeOH (96:4) as eluent. Solvent removal in vacuo gave 0.76 g (64%) of the title compound as a colorless oil. HRMS m/z for C13H16N4OS (M)+ calcd for 276.1045, found 276.1037. Anal. (C13H16N4OS.0.25 H2O) C, H, N.

Aufarbeitung

  1. customThe title compound was prepared
  2. customwere evaporated off
  3. dissolutionThe remaining oil was redissolved in ethyl acetetate
  4. filtrationfiltered through a short plug of alumina (5×3 cm)
  5. customSolvent removal in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-b249145950ec465ea3bfa00bacdcc500
Quelldatensatz
uspto-grants-2007_07
Patentnummer
US07247633B2

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