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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415600Generated: October 31, 2026

HCID 178500499, compound → 8-chloro-6-(o-chlorophenyl)-2-methyl-4H-imidazo[1,2-a][1,4]benzodiazepine

https://huagongshe.com/reaction/1415600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178500499HCID 178500499—
CatalystTitanium TetrachlorideHCID 24193—
Solvent1,2-DimethoxyethaneHCID 8071—
Product8-chloro-6-(o-chlorophenyl)-2-methyl-4H-imidazo[1,2-a][1,4]benzodiazepineHCID 12707131—

Reaction Steps

A sample of 2-[[7-chloro-5-(o-chlorophenyl)-3H-1,4-benzodiazepin-2-yl]amino]propionaldehyde dimethyl acetal (2.03 g., 5.00 mmol), dissolved in 60 ml. of monoglyme, is treated with 0.75 ml. (1.30 g., 6.85 mmol) of (reagent-grade) titanium tetrachloride. A vigorous reaction takes place and a brown solid precipitates in the reaction flask. The mixture is refluxed under nitrogen for 4 hours. The reaction mixture is cooled to room temperature, poured into 250 ml. of cold 5% aqueous sodium hydroxide and extracted with chloroform (400 ml.). The chloroform layer is washed with brine, dried over anhydrous magnesium sulfate and concentrated in vacuo to a solid. After crystallization 960 mg. of 8-chloro-2-methyl-6-(o-chlorophenyl)-4H-imidazo[1,2-a][1,4]-benzodiazepine of melting point 169.5° -170.5° C. is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04005099
Source datasetuspto-grants-1977_01
ORD IDord-ac9c1104d3ab49b2a99b1e96adea2cc1
Source noteuspto-grants-1977_01