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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1760046Generated: October 31, 2026

Tetrafluoroboric acid → HCID 69743175, compound

https://huagongshe.com/reaction/1760046

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrafluoroboric acidHCID 28118—
Reactant1,4-DioxaneHCID 31275—
ReactantHCID 20748464HCID 20748464—
ReactantSodium NitriteHCID 23668193—
CatalystHCID 178419072HCID 178419072—
SolventWaterHCID 962—
ProductHCID 69743175HCID 6974317571.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06838465B2
Source datasetuspto-grants-2005_01
ORD IDord-4445743d773743b89cf88c177901d8de
Source noteuspto-grants-2005_01