Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758781Generated: November 2, 2026

Sodium Hydroxide → 8-amino-6-(o-fluorophenyl)-1,4,4-trimethyl-4H-s-triazolo[4,3-a][1,4]benzodiazepine

https://huagongshe.com/reaction/1758781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantTin tetrachlorideHCID 24287—
Reactant6-(o-fluorophenyl)-1,4,4-trimethyl-8-nitro-4H-s-triazolo[4,3-a][1,4]benzodiazepineHCID 20508539—
SolventHydrochloric AcidHCID 313—
Product8-amino-6-(o-fluorophenyl)-1,4,4-trimethyl-4H-s-triazolo[4,3-a][1,4]benzodiazepineHCID 20508558—

Reaction Steps

43.6 g (0.12 mol) of 6-(o-fluorophenyl)-1,4,4-trimethyl-8-nitro-4H-s-triazolo[4,3-a][1,4]benzodiazepine in 600 ml of concentrated hydrochloric acid are treated portionwise with a total of 80.55 g (0.36 mol) of tin chloride in such a manner that the temperature of the mixture does not exceed 85° C. Subsequently, the mixture is stirred at room temperature for 1 hour, cooled to 0° C. and cautiously neutralised with 900 ml of 10 N sodium hydroxide. After extracting the remaining suspension three times with methylene chloride, the combined organic phases are washed with saturated sodium chloride solution, dried and evaporated. Recrystallisation of the residue from 350 ml of ethanol at -30° C. gives 8-amino-6-(o-fluorophenyl)-1,4,4-trimethyl-4H-s-triazolo[4,3-a][1,4]benzodiazepine of melting point 294° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04374773
Source datasetuspto-grants-1983_02
ORD IDord-c8980772c9734e4c859d797f6929f8bd
Source noteuspto-grants-1983_02