HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1760046Generated: October 31, 2026
Tetrafluoroboric acid → HCID 69743175, compound
https://huagongshe.com/reaction/1760046
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrafluoroboric acid | HCID 28118 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 20748464 | HCID 20748464 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Catalyst | HCID 178419072 | HCID 178419072 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 69743175 | HCID 69743175 | 71.1% |
Reaction Steps
Tetrafluoroboric acid (1.5 ml) and an aqueous sodium nitrite solution (20 mg/0.2 ml, 0.29 mmol) were added, at 0° C., to a dioxane (2 ml) solution of (2S)-2-[(2aminophenyl)amino]-1-(6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolin-2-yl)-3,3dimethylbutan-1-one (100 mg, 0.25 mmol) obtained in Example 25, and the mixture was stirred at that temperature for 30 minutes. Copper (I) oxide (75 mg, 0.52 mmol) was added to the reaction solution, and the mixture was stirred for 30 minutes. Dioxane (2 ml) and water (10 ml) were added to the mixture, and the mixture was concentrated under reduced pressure. The residue was extracted twice with chloroform (each 5 ml), and the extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel thin layer chromatography using hexane and ethyl acetate (2:1) as an eluent to obtain the captioned compound (68.0 mg, 70%) as a green oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06838465B2 |
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| Source dataset | uspto-grants-2005_01 |
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| ORD ID | ord-4445743d773743b89cf88c177901d8de |
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| Source note | uspto-grants-2005_01 |
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