HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350462Generated: November 1, 2026
Methyl triflate → (S)-10-{3-[2-(4-Fluoro-phenyl)-ethyl]-piperazin-1-yl}-2-isopropyl-4H-3-thia-1,4,9-triaza-benzo[f]azulene
https://huagongshe.com/reaction/1350462
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl triflate | HCID 9526 | — |
| Reactant | 2-Isopropyl-4,9-dihydro-3-thia-1,4,9-triazabenzo[f]azulene-10-thione | HCID 21093479 | — |
| Reactant | (S)-2-(2-(4-Fluoro-phenyl)-ethyl)-piperazine | HCID 69487151 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ammonia methanol | HCID 21705897 | — |
| Product | (S)-10-{3-[2-(4-Fluoro-phenyl)-ethyl]-piperazin-1-yl}-2-isopropyl-4H-3-thia-1,4,9-triaza-benzo[f]azulene | HCID 136005614 | 78.7% |
Reaction Steps
Stir 2-isopropyl-4,9-dihydro-3-thia-1,4,9-triaza-benzo[f]azulene-10-thione (0.551 g, 2.0 mmol) in dichloromethane (10.0 mL) and chilled in an ice bath while adding methyl trifluoromethane sulfonate (0.27 mL, 2.4 mmol). Allow this solution to stir at ambient temperature for 16 hours. Evaporate the solvent to a gray solid. Dissolve this solid and (S)-2-[2-(4-fluoro-phenyl)-ethyl]-piperazine (0.417 g, 2.0 mmol) in pyridine (8.0 mL) and heat at 115° C. for 23 hours. After evaporation of the pyridine, silica gel chromatography, eluting with methylene chloride: 2N NH3/methanol (100:5), gives 0.354 g of the title compound as a yellow solid: mass spectrum (ion spray): m/z=450 (M+1); Analysis for C25H28FN5S(0.2 H2O): calcd: C, 66.26; H, 6.32; N, 15.45; found: C, 66.01; H, 6.15; N, 15.25.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07214673B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-4ae1470cffe742eea7750ceda4dc7fd8 |
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| Source note | uspto-grants-2007_05 |
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