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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 441940Erstellt: 24. Oktober 2026

Ammonia → Medazepam

https://huagongshe.com/de/reaction/441940

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
EduktHydrochloric AcidHCID 313—
EduktDiazepamHCID 3016—
EduktBoron trifluoride etherateHCID 8000—
EduktSodium borohydrideHCID 4311764—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMedazepamHCID 4041103%

Reaktionsschritte

To a suspension of 2.28 g of sodium borohydride in 35ml of tetrahydrofuran was added dropwise with stirring a solution of 13.0 g of boron trifluoride etherate in 10ml of tetrahydrofuran below 10° C, and the mixture was stirred at room temperature for 45 minutes. To the mixture was added dropwise solution of 1.43 g of 1-methyl-5-phenyl-7-chloro-1,3-dihydro-2H-1,4-benzodiazepin-2-one in 10 ml of tetrahydrofuran at -15° to -12.5° C over a period of 5 minutes, and then the mixture was stirred at =15° C for 22 hours. The reaction mixture was poured into 100 ml of ice-water, and then 20 ml of concentrated hydrochloric acid was added. The mixture was refluxed for 30 minutes, then cooled, and neutralized with concentrated ammonia. The tetrahydrofuran layer was separated, and the aqueous layer was extracted with ether. The combined organic layer was washed with water and dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure to obtain 1.4 g of 1-methyl-5-phenyl-7-chloro-2,3-dihydro-1H-1,4-benzodiazepine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04044003
Quelldatensatzuspto-grants-1977_08
ORD IDord-f477172c64e844b98d04e50fc6afdfa7
Quellennotizuspto-grants-1977_08