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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986563Generated: October 30, 2026

Hydrochloric Acid → 8-Chloro-5-methyl-11-(piperazin-1-yl)-5H-dibenzo[b,e][1,4]diazepine

https://huagongshe.com/reaction/1986563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPiperazineHCID 4837—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant8,5-Dichloro-5H-dibenzo[b,e][1,4]diazepineHCID 57485431—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product8-Chloro-5-methyl-11-(piperazin-1-yl)-5H-dibenzo[b,e][1,4]diazepineHCID 1118645354.8%

Reaction Steps

NaH (12 mg, 0.29 mmol, 60% in mineral oil) was added to a mixture of 8,5-dichloro-5H-dibenzo[b,e][1,4]diazepine (160FE64) (50 mg, 0.19 mmol) in toluene (1.5 mL) and DMF (0.5 mL). MeI (24 μL, 0.38 mmol) was then added. The resulting mixture was stirred for 1 h then quenched by addition of saturated aqueous NaHCO3-solution (2 mL). The mixture was extracted with diethyl ether, and the combined organic phases were dried (Na2SO4) and concentrated. The residue was taken up in toluene (2.0 mL), piperazine (98 mg, 1.1 mmol) was added, and the resulting mixture was stirred at 100° C. for 1 h. Aqueous HCl (1 mL, 2M) and EtOAc (2 mL) was then added to the mixture. The phases were separated and the aqueous phase was extracted with EtOAc (2 mL) and then aqueous NaOH (2 mL, 2 M) was added. The basic aqueous phase was extracted with EtOAc (3×2 mL) and the combined organic phases were dried (Na2SO4) and concentrated. The residue was dissolved in DMF and purified on HPLC to give 34 mg of the title compound (189JO25A). MS (ESI) 327 (MH+). Purity for MH+ (UV/MS) 100/100.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07550454B2
Source datasetuspto-grants-2009_06
ORD IDord-18139bd642ec4ed5ba9a4136975baf1e
Source noteuspto-grants-2009_06