HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 86664798, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | HCID 86664797 | HCID 86664797 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Product | HCID 86664798 | HCID 86664798 | — |
Reaction Steps
This material, tert-butyl (1-benzylpiperidin-4-yl)methyl(7-(bis((2-(trimethylsilyl)ethoxy)methyl)amino)-3-(6-fluoroquinolin-3-yl)pyrazolo[1,5-a]pyrimidin-5-yl)carbamate, was then stirred with Pd(OH)2/C (0.2 equiv) and ammonium formate (20 equiv) in ethanol at 80° C. until the reaction was deemed complete by HPLC, LC-MS, or TLC analysis. The mixture was allowed to cool to room temperature, filtered through a pad of celite, concentrated and purified on silica gel to afford compound tea-butyl 7-(bis((2-(trimethylsilyl)ethoxy)methyl)amino)-3-(6-fluoroquinolin-3-yl)pyrazolo[1,5-a]pyrimidin-5-yl(piperidin-4-ylmethyl)carbamate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08591943B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-b627ed6af6864384a0c9cccb9e09f7bd |
| Source note | uspto-grants-2013_11 |