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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436133Generated: October 27, 2026

Sodium hydride → 4,9-Dihydro-9-(3-dimethylaminopropyl)-4-methyl-10H-thieno[3,4-b][1,5]benzodiazepin-10-one

https://huagongshe.com/reaction/436133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant3-Chloro-N,N-dimethyl-1-propanamineHCID 66960—
Reactant4,9-Dihydro-4-methyl-10H-thieno[3,4-b][1,5]benzodiazepin-10-oneHCID 12521642—
SolventDimethylformamideHCID 6228—
Product4,9-Dihydro-9-(3-dimethylaminopropyl)-4-methyl-10H-thieno[3,4-b][1,5]benzodiazepin-10-oneHCID 21455234—

Reaction Steps

A mixture of 0.3 g. of 55% sodium hydride-mineral oil dispersion and 0.35 g. of 4,9-dihydro-4-methyl-10H-thieno-[3,4-b][1,5]benzodiazepin-10-one in 25 ml. of dry dimethylformamide is stirred at room temperature for 0.5 hours. To the mixture is added 0.45 g. of dimethylaminopropyl chloride 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 under reduced pressure to give an oil which is crystallized by dissolving in boiling hexane and a minimal volume of ethyl acetate and cooling to give off-white crystals, m.p. 52°-56° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04007272
Source datasetuspto-grants-1977_02
ORD IDord-303f42ecf635484681fd45d15d6b92dc
Source noteuspto-grants-1977_02