HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131450Generated: October 31, 2026
Dimethyl Sulfoxide → (S)-6,7-Difluoro-10-[3-(2-methoxy-ethyl)-piperazin-1-yl]-4H-3-thia-4,9-diaza-benzo[f]azulene
https://huagongshe.com/reaction/131450
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | (S)-2-(2-Methoxyethyl)piperazine | HCID 55287560 | — |
| Reactant | HCID 136388578 | HCID 136388578 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (S)-6,7-Difluoro-10-[3-(2-methoxy-ethyl)-piperazin-1-yl]-4H-3-thia-4,9-diaza-benzo[f]azulene | HCID 135516879 | 49% |
Reaction Steps
Combine 6,7-difluoro-4H-3-thia-4,9-diaza-benzo[f]azulen-10-ylamine hydrochloride (876.9 mg, 3.05 mmol), (S)-2-(2-methoxy-ethyl)-piperazine (1.32 g, 9.16 mmol), DMSO (3.0 ml), and toluene (12.0 ml). Stir and heat the mixture at 105° C. After 63 hours, cool the mixture to ambient temperature. Dilute the mixture with ethyl acetate and wash the organic layer with 1N NaOH and brine. Dry (sodium sulfate) and concentrate the organic layer to residue. Purify the residue on silica gel using a gradient of dichloromethane to dichloromethane/methanol (85:15) to give 561.6 mg (49%) of the title compound: mass spectrum (ion spray): m/z=379.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07384934B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-9df05e806ebb4709b3342d7218e5225a |
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| Source note | uspto-grants-2008_06 |
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