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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863188Generated: October 31, 2026

Potassium Iodide → 9-[4-chloro-3-(trifluoromethyl)benzyl]-4,9-dihydro-10H-thieno[3,4-b][1,5]benzodiazepin-10-one

https://huagongshe.com/reaction/1863188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium hydrideHCID 24758—
Reactant4,9-dihydro-10H-thieno[3,4-b][1,5]benzodiazepin-10-oneHCID 12521641—
Reactant1-Chloro-4-(chloromethyl)-2-(trifluoromethyl)benzeneHCID 13094262—
SolventDimethylformamideHCID 6228—
Product9-[4-chloro-3-(trifluoromethyl)benzyl]-4,9-dihydro-10H-thieno[3,4-b][1,5]benzodiazepin-10-oneHCID 20392258—

Reaction Steps

To a solution of 8.64 g. of 4,9-dihydro-10H-thieno[3,4-b][1,5]benzodiazepin-10-one in 100 ml. of dimethylformamide is added 2.1 g. of 50% sodium hydride in mineral oil. The mixture is stirred for one hour and 10.0 g. of 4-chloro-3-trifluoromethyl benzyl chloride and 10 mg of potassium iodide are added. The mixture is stirred for a prolonged period and the solvent is removed in vacuo. The residual gum is dissolved in methylene chloride, dried over magnesium sulfate and filtered through magnesol. The filtrate is evaporated to give tan crystals which are recrystallized from ethanol giving the desired product as off-white crystals, mp. 181°-183° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04168269
Source datasetuspto-grants-1979_09
ORD IDord-4b9804bd98b641c691ff56b341ba740a
Source noteuspto-grants-1979_09