HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-butyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)allylcarbamate → HCID 57590905, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-butyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)allylcarbamate | HCID 11818401 | — |
| Reactant | 6-Bromo-9-chloro-1,2,4-triazolo[3,4-a]isoquinolin-3(2H)-one | HCID 57590862 | — |
| Solvent | Potassium Carbonate | HCID 11430 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 57590905 | HCID 57590905 | — |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
6-bromo-9-chloro[1,2,4]triazolo[3,4-a]isoquinolin-3(2H)-one (3-9) (60 mg, 0.201 mmol, 1.0 equiv.) and tert-butyl[(2E)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)prop-2-en-1-yl]carbamate (3-3) (228 mg, 0.804 mmol, 4.0 equiv.) were dissolved in anhydrous 1,4-dioxane (0.6 ml) and 2 M K2CO3 aqueous solution (0.2 mL). The reaction mixture was heated to 100° C. LCMS at 18 hours showed complete conversion. Purification with reverse phase HPLC (H2O/CH3CN gradient w/0.1% TFA) afforded the title product 3-10. LRMS m/z (M+H) 375.1 found, 375.1 required.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07501435B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-d866d13c699e425cadf4e782d6af76db |
| Source note | uspto-grants-2009_03 |