Trifluoroacetic acid → HCID 178513859, Verbindung

HRID 614239Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 614239
[C:1]([C:4]1[N:8](CC2C=CC(OC)=CC=2)[C:7]([SH:18])=[N:6][N:5]=1)(=[O:3])[NH2:2].FC(F)(F)C(O)=O.C1(OC)C=CC=CC=1>>[C:1]([C:4]1[N:8]=[C:7]([SH:18])[NH:6][N:5]=1)(=[O:3])[NH2:2]

Komponenten

4

Versuchsvorschrift

3-Carbamoyl-4-(p-methoxybenzyl)-1,2,4-triazole-5-thiol (2.0 g., 0.007 mole), trifluoroacetic acid (8 ml.) and anisole (2 ml.) were heated at 70° C. for 3.5 hours. At this point, most of the trifluoroacetic acid present was removed by means of evaporation under reduced pressure and the residue was subsequently triturated with diethyl ether. The resulting solid was then filtered, washed with diethyl ether and subsequently dried in vacuo at 50° C. to give pure 3-carbamoyl-1,2,4-triazole-5-thiol (1.0 g., 91% yield), m.p. 276°-278° C. The infrared absorption spectrum was identical to that of a reference sample prepared as described in Example XVI, Part C.

Aufarbeitung

  1. customAt this point, most of the trifluoroacetic acid present was removed by means of evaporation under reduced pressure
  2. customthe residue was subsequently triturated with diethyl ether
  3. filtrationThe resulting solid was then filtered
  4. washwashed with diethyl ether
  5. customsubsequently dried in vacuo at 50° C.

Quellen und Nachweise

ORD-Eintrag
ord-77bcf13f046c47699832f71af0b71d92
Quelldatensatz
uspto-grants-1979_03
Patentnummer
US04144240

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