HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281795Generated: November 1, 2026
1-Methylpiperazine → 8-fluoro-12-(4-methylpiperazin-1-yl)-6H-(1)benzothieno(2,3-b)(1,5)benzodiazepine
https://huagongshe.com/reaction/1281795
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | Ethyl 2-(2-amino-5-fluoroanilino)benzo[b]thiophene-3-carboxylate | HCID 18422159 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Anisole | HCID 7519 | — |
| Product | 8-fluoro-12-(4-methylpiperazin-1-yl)-6H-(1)benzothieno(2,3-b)(1,5)benzodiazepine | HCID 9913124 | — |
Reaction Steps
Ethyl 2-(2-amino-5-fluoroanilino)benzo[b]thiophene-3-carboxylate (24.5 g) and 1-methylpiperazine (135 ml) were dissolved in anisole (400 ml), and titanium tetrachloride (21 ml) was added dropwise while stirring the mixture at room temperature. After the completion of the dropwise addition, the mixture was stirred at 140° C. for 17 hours. The reaction mixture was cooled to 80° C. and poured into ice water. The resultant precipitate was filtrated and the filtrate was extracted with ethyl acetate, washed with saturated brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/methanol) and the obtained oily substance (17 g) was dissolved in ethyl acetate (400 ml). Thereto was added a solution of maleic acid (5.9 g) in ethyl acetate (100 ml) and ethanol (20 ml). The precipitated crystals were collected by filtration and recrystallized from ethanol to give 8-fluoro-12-(4-methylpiperazin-1-yl)-6H-[I]benzothieno[2,3-b][1,5]benzodiazepine.1 maleate (10.2 g).
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-f09cc590e14a49468e8e612ff06292f3 |
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| Source note | uspto-grants-2002_09 |
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