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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 234824Erstellt: 26. Oktober 2026

Hydrazine → HCID 178427630, Verbindung

https://huagongshe.com/reaction/234824

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrazineHCID 9321—
EduktDiisopropylethylamineHCID 81531—
EduktN-Boc-2-chloroethylamineHCID 3795708—
Edukt9-Fluoro-6-(p-toluenesulfonyloxy)benzo[g]isoquinoline-5,10-dioneHCID 10572880—
Edukt9-Chloro-6-(p-toluenesulfonyloxy)benzo[g]isoquinoline-5,10-dioneHCID 19974754—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 178427630HCID 178427630—

Reaktionsschritte

(2-N-tert-butoxycarbonylaminoethyl)hydrazine is prepared by reaction of N-t-butoxycarbonyl-2-chloro-ethylamine with hydrazine following a procedure adapted from J. Med. Chem. 7, 493, (1964). Under a nitrogen atmosphere a solution of (2-N-tert-butoxycarbonylaminoethyl)hydrazine (9.2 g) in anhydrous THF (10 mL) is added during 30' to the stirred 9:1 mixture of 9-fluoro-6-(p-toluenesulfonyloxy)benzo[g]isoquinoline-5,10-dione and 9-chloro-6-(p-toluenesulfonyloxy)benzo [g]isoquinoline-5,10-dione of Preparative Example 15b (3.0 g) in THF (25 mL) containing N,N-diisopropylethylamine (1.38 mL). A slightly exothermic reaction ensues, and the reaction temperature increases from 21° C. to 24° C. After stirring for one hour at room temperature the obtained precipitate is recovered by suction, washed with THF/n-hexane 1/1 (15 mL) and dried at 40° C. under vacuum, to give 2-[2-(N-tert-butoxycarbonylamino)ethyl[-5-(p-toluenesulfonyloxy)iso-quino[8,7,6-cd]indazole-6(2H)-one (1.33 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05596097
Quelldatensatzuspto-grants-1997_01
ORD IDord-d8fd736de86e4c2b8e3db1257e6b8df0
Quellennotizuspto-grants-1997_01