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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436132Generated: October 27, 2026

Sodium hydride → 4,9-Dihydro-9-(2-dimethylaminoathyl)-4-methyl-thieno[3,4-b][1,5]benzodiazepin-10-on

https://huagongshe.com/reaction/436132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantN,N-Dimethylaminoethyl chloride hydrochlorideHCID 11636816—
Reactant4,9-Dihydro-4-methyl-10H-thieno[3,4-b][1,5]benzodiazepin-10-oneHCID 12521642—
SolventDimethylformamideHCID 6228—
Product4,9-Dihydro-9-(2-dimethylaminoathyl)-4-methyl-thieno[3,4-b][1,5]benzodiazepin-10-onHCID 21455235—

Reaction Steps

A mixture of 0.4 g. of 55% sodium hydride-mineral oil dispersion 0.5 g. of 2-dimethylaminoethylchloride hydrochloride and 25 ml. of dry dimethylformamide is stirred at room temperature for 0.5 hours. To the mixture is added 0.4 g. of 4,9-dihydro-4-methyl-10H-thieno[3,4-b][1,5]benzodiazepin-10-one and stirring at room temperature is continued for 18 hours. The reaction mixture is cooled, quenched with water, acidified, decolorized and filtered. The filtrate is made alkaline and extracted with chloroform. The dried chloroform extracts are concentrated to give a solid which is recrystallized from chloroform-hexane to give off-white crystals, m.p. 147°-149° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04007272
Source datasetuspto-grants-1977_02
ORD IDord-c9e7d6ef85e841e3adf6f9cc812d07ff
Source noteuspto-grants-1977_02