HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281821Generated: October 28, 2026
HCID 18422180, compound → HCID 18422168, compound
https://huagongshe.com/reaction/1281821
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 18422180 | HCID 18422180 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 18422168 | HCID 18422168 | 136.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06455521B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-ae6fada4b2c64ccd9fd73ad2ff5f3bc3 |
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| Source note | uspto-grants-2002_09 |
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