Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731084Generated: November 1, 2026

Ethyl Acetate → 1-(2-aminoethyl)-8-chloro-6-phenyl-4H-s-triazolo[4,3-a][1,4]benzodiazepine

https://huagongshe.com/reaction/1731084

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant8-chloro-6-phenyl-1-(2-phthalimidoethyl)-4H-s-triazolo[4,3-a][1,4]benzodiazepineHCID 12612391—
SolventEthanolHCID 702—
Product1-(2-aminoethyl)-8-chloro-6-phenyl-4H-s-triazolo[4,3-a][1,4]benzodiazepineHCID 12612403—

Reaction Steps

A stirred mixture of 8-chloro-6-phenyl-1-(2-phthalimidoethyl)-4H-s-triazolo[4,3-a][1,4]benzodiazepine, ethyl acetate solvate (37.6 g., 0.0675 mole) and absolute ethanol (340 ml.) is treated with hydrazine hydrate (7.43 g.) and warmed, under nitrogen, in an oil bath to 75° during 65 minutes, the bath is kept at this temperature for an additional 55 minutes. The mixture is then cooled in an ice bath, and the solid is collected by filtration and washed with absolute ethanol and methylene chloride. The combined filtrate is mixed with ice cold salt water and extracted with methylene chloride. The extract is washed with water, dried over anhydrous sodium sulfate and concentrated in vacuo. The residue is chromatographed on silica gel (1 kg.) with methanol and the resulting product is crystallized from methylene chloride diethyl ether to give 1-(2-aminoethyl)-8-chloro-6-phenyl-4H-s-triazolo-[4,3-a][1,4]benzodiazepine in 2 crops: 5.29 g. of melting point 198°-200° C. dec., and 2.37 g., of melting point 194°-196.5° C. dec. The analytical sample is crystallized from methanol-ethyl acetate and has a melting point of 205°-207° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03994941
Source datasetuspto-grants-1976_11
ORD IDord-4a692b6968144860914d7253eed7c227
Source noteuspto-grants-1976_11