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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704555Generated: October 30, 2026

Clobazam → 1-Methyl-5-phenyl-1H-1,5-benzodiazepine-2,4(3H,5H)-dione

https://huagongshe.com/reaction/704555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantClobazamHCID 2789—
ReactantPotassium HydroxideHCID 14797—
SolventMethanolHCID 887—
Product1-Methyl-5-phenyl-1H-1,5-benzodiazepine-2,4(3H,5H)-dioneHCID 1469765784.1%

Reaction Steps

A suspension of 103 g of clobazam, 1 liter of methanol, 23 g of potassium hydroxide in solution in 400 ml of methanol and 50 g of Raney's nickel washed beforehand with water and with methanol, was hydrogenated for 24 hours under a pressure of 800 mbars. 1 liter of methylene chloride was added and the catalyst was filtered off. The solvents were concentrated under reduced pressure and the residue was taken up in methylene chloride. The mixture was washed with water, dried over magnesium sulfate and concentrated under reduced pressure. The product obtained was crystallized from methanol, washed with ether and dried to obtain 76.69 g of the sought product melting at 173° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04988692
Source datasetuspto-grants-1991_01
ORD IDord-79c2a93c1fcf4fbfb5ed262181f47bfa
Source noteuspto-grants-1991_01