Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769112Generated: October 25, 2026

Methyl iodide → 4,5-Dihydro-4-methyl-3-methylthio-1-phenyl-1H-2,4-benzodiazepine

https://huagongshe.com/reaction/1769112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant1,2,4,5-Tetrahydro-4-methyl-1-phenyl-3H-2,4-benzodiazepin-3-thioneHCID 14978307—
SolventEthanolHCID 702—
Product4,5-Dihydro-4-methyl-3-methylthio-1-phenyl-1H-2,4-benzodiazepineHCID 1497830861.4%

Reaction Steps

A solution of 8 g (30 mmol) of the thione of Example 152 and 2.7 mL (44 mmol) of methyl iodide in 100 mL of ethanol was refluxed two hours, cooled, and the hydriodide of the product filtered off. The salt was partitioned between methylene chloride and aqueous sodium bicarbonate, the organic layer dried over magnesium sulfate, and stripped. The residue was dissolved in ethanol and 2.7 g of methanesulfonic acid was added followed by ether. The resulting precipitate was filtered off and recrystallized from ethanol to yield 5.2 g of product as the methanesulfonate salt, mp 195-196.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05380721
Source datasetuspto-grants-1995_01
ORD IDord-4e62f45d78e54a29bd6d1064583ed0ad
Source noteuspto-grants-1995_01