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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834372Generated: October 31, 2026

Methyl iodide → 2-(methylthio)-7-chloro-5-phenyl-3H-1,5-benzodiazepin-4-one

https://huagongshe.com/reaction/1834372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium HydroxideHCID 14798—
Reactant7-chloro-5-phenyl-1H-1,5-benzodiazepin-4-one-2-thioneHCID 12264319—
SolventMethanolHCID 887—
Product2-(methylthio)-7-chloro-5-phenyl-3H-1,5-benzodiazepin-4-oneHCID 20329323—

Reaction Steps

To 3.03 g of 7-chloro-5-phenyl-1H-1,5-benzodiazepin-4-one-2-thione in a solution of 0.40 g of sodium hydroxide and 15 ml of methanol is added, with stirring a solution of 1.4 g of methyl iodide in 10 ml of methanol. Stirring is continued for 1 hour, the reaction is then evaporated and suspended in methylene chloride (30 ml). The suspension is filtered through a short Florisil column; the column is washed with ethyl acetate and the combined filtrates are evaporated. The residue is triturated with a minimum amount of absolute ethanol and the title compound is filtered off and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04070355
Source datasetuspto-grants-1978_01
ORD IDord-1f7f0f4a31b24cb3b98faf2336c3e880
Source noteuspto-grants-1978_01