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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281821Generated: October 28, 2026

HCID 18422180, compound → HCID 18422168, compound

https://huagongshe.com/reaction/1281821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18422180HCID 18422180—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 18422168HCID 18422168136.4%

Reaction Steps

8-Fluoro-12-(4-tert-butoxycarbonylpiperazin-1-yl)-6H-[1]benzothieno[2,3-b][1,5]benzodiazepine (1.6 g) was dissolved in trifluoroacetic acid (8 ml) and the mixture was stirred at room temperature for 3 hours. Trifluoroacetic acid was evaporated under reduced pressure. The residue was dissolved in ethyl acetate and saturated aqueous sodium hydrogencarbonate solution was added. The mixture was stirred at room temperature for 2 hours and the ethyl acetate layer was dried over magnesium sulfate. After natural filtration, the solvent was evaporated and the residue was separated and purified by silica gel column chromatography (chloroform:methanol=4:1) to give 8-fluoro-12-(piperazin-1-yl)-6H-[1]benzothieno[2,3-b][1,5]benzodiazepine (1.7 g), which was treated with maleic acid to give 8-fluoro-12-(piperazin-1-yl)-6H-[1]benzothieno[2,3-b][1,5]benzodiazepine.3/2 maleate.1/2 hydrate (347 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455521B1
Source datasetuspto-grants-2002_09
ORD IDord-ae6fada4b2c64ccd9fd73ad2ff5f3bc3
Source noteuspto-grants-2002_09