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HRID 25943Erstellt: 24. Oktober 2026

Diethyl Ether → 5-chloro-2-(3-glycylaminomethyl-4H-1,2,4-triazol-4-yl)-benzophenone

https://huagongshe.com/de/reaction/25943

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
Edukt5-chloro-2-[3-(N-carbobenzoxyglycyl)aminomethyl-4H-1,2,4-triazol-4-yl]-benzophenoneHCID 21325675—
LösungsmittelAnisoleHCID 7519—
LösungsmittelAcetic Acid Mixture with Hydrobromic AcidHCID 21893785—
Produkt5-chloro-2-(3-glycylaminomethyl-4H-1,2,4-triazol-4-yl)-benzophenoneHCID 1556787925,3%

Reaktionsschritte

To a solution of 5-chloro-2-[3-(N-carbobenzoxyglycyl)aminomethyl- 4H-1,2,4-triazol-4-yl]-benzophenone (2.1 g) in anisole (4 ml), 30% hydrogen bromide-acetic acid is added. The resultant mixture is stirred for 1 hour and mixed with ether. The precipitate is filtered, washed with ether and dissolved in methylene chloride (20 ml). The methylene chloride layer is washed with saturated aqueous sodium bicarbonate, water and saturated aqueous saline solution in order, dried over sodium sulfate and evaporated under reduced pressure to remove the solvent. The residue is chromatographed on a column of silica gel, which is eluted with methanol to give 5-chloro-2-(3-glycylaminomethyl-4H-1,2,4-triazol-4-yl)-benzophenone as a colorless oil (0.39 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04147700
Quelldatensatzuspto-grants-1979_04
ORD IDord-49a9e395c62149e480268ee11be954a5
Quellennotizuspto-grants-1979_04