HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrabutylammonium Fluoride → HCID 89812915, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 89812812 | HCID 89812812 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 89812915 | HCID 89812915 | 100% |
Reaction Steps
To a stirred solution of 4-[4-(1-oxo-5-trimethylsilanylethynyl-1,2-dihydroisoquinolin-3-yl)benzyl]piperazine-1-carboxylic acid tert-butyl ester compound (70.0 mg, 0.136 mmol) in THF (5 mL) was added TBAF (1M in THF, 272 μL, 0.272 mmol). The resulting reaction mixture was stirred at RT for 2 h and then quenched by the addition of water (20 mL). The mixture was extracted with EtOAc (3×20 mL) and the combined organic layer was washed with brine (50 mL), dried over Na2SO4, filtered and concentrated in vacuo to obtain 4-[4-(5-ethynyl-1-oxo-1,2-dihydroisoquinolin-3-yl)benzyl]piperazine-1-carboxylic acid tert-butyl ester (60.3 mg, 100%) as an orange solid. The crude compound was used for the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09193689B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-46cdfc7b73a548159b4c5b67bc50ad69 |
| Source note | uspto-grants-2015_11 |