Ammonia → 5-(Piperazin-1-yl)benzofuran-2-carboxamide

HRID 1056548

Reaktionsgleichung

Reaktionsgleichung von HRID 1056548
[N:1]1([C:7]2[CH:8]=[CH:9][C:10]3[O:14][C:13]([C:15](OC)=[O:16])=[CH:12][C:11]=3[CH:19]=2)[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.[NH3:20].Cl>O>[N:1]1([C:7]2[CH:8]=[CH:9][C:10]3[O:14][C:13]([C:15]([NH2:20])=[O:16])=[CH:12][C:11]=3[CH:19]=2)[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1

Komponenten

5

Edukt 3

HCID 222AmmoniaHCID 313Hydrochloric AcidHCID 77231352Methyl 5-(piperazin-1-yl)benzofuran-2-carboxylate

Produkt 1

HCID 98347195-(Piperazin-1-yl)benzofuran-2-carboxamideAusbeute 73,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

Methyl 5-(1-piperazinyl)benzofuran-2-carboxylate (37 g) was added to saturated methanolic ammonia solution (1850 ml) at 25-30° C., the mixture was stirred for 6 to 16 hours at the same temperature. The reaction mass was distilled under vacuum to remove the solvent after completion of the reaction. Water (148 ml) was added to the resulting residue, followed by adjusting the pH to 2-4 with concentrated HCl and then filtering the aqueous layer. The pH of the resulting aqueous layer was adjusted to 9-10 with ammonium hydroxide solution. The separated solid was filtered, washed with water (100 ml) and then dried to produce 25.5 g of 5-(1-piperazinyl)benzofuran-2-carboxamide (Purity by HPLC: 99%; Yield: 73.1%).

Aufarbeitung

  1. distillationThe reaction mass was distilled under vacuum
  2. customto remove the solvent
  3. customafter completion of the reaction
  4. filtrationfiltering the aqueous layer
  5. filtrationThe separated solid was filtered
  6. washwashed with water (100 ml)
  7. customdried

Quellen und Nachweise

ORD-Eintrag
ord-c16dad9cfd714f6abcc66ba4f2029e7f
Quelldatensatz
uspto-grants-2016_07
Patentnummer
US09399630B2

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