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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606443Generated: October 25, 2026

Hydrochloric Acid → 9-(3-Dimethylamino-2-methylpropyl)-4,9-dihydro-4-methyl-10H-thieno[3,4-b][1,5]benzodiazepin-10-one, hydrochloride

https://huagongshe.com/reaction/1606443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant3-Chloro-2-methylpropyl(dimethyl)ammonium chlorideHCID 3083841—
ReactantHCID 12521642HCID 12521642—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product9-(3-Dimethylamino-2-methylpropyl)-4,9-dihydro-4-methyl-10H-thieno[3,4-b][1,5]benzodiazepin-10-one, hydrochlorideHCID 131710151—

Reaction Steps

A mixture of 0.47 g. of 55% sodium hydride-mineral oil dispersion and 0.91 g. of 3-dimethylamino-2-methylpropylchloride hydrochloride in 35 ml. of dry dimethylformamide is stirred at room temperature for 0.5 hours. To the mixture is added 0.6 g. of 4,9-dihydro-4-methyl-10H-thieno[3,4-b] [1,5]benzodiazepin-10-one and stirring is continued for 18 hours. The reaction mixture is cooled, quenched with water and extracted with chloroform. The dried chloroform extracts are concentrated to an oil, which is chromatographed on silica gel preparative thin layer chromatographic (tlc) plates with 10:1 benzene:methanol to give an oil. An ethanolic solution of the oil is treated with anhydrous hydrogen chloride and diluted with ether to give a white solid, m.p. 231°-233°C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03953430
Source datasetuspto-grants-1976_04
ORD IDord-d42903d7e4004faf9a0146dd104446c8
Source noteuspto-grants-1976_04