Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | tert-butyl (2,3-dihydro(1,4)dioxino(2,3-c)pyridin-7-ylmethyl)(1-(2-(7-fluoro-2-oxo-1,5-naphthyridin-1(2H)-yl)ethyl)piperidin-4-yl)carbamate | HCID 57815262 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 68672939 | HCID 68672939 | — |
Reaction Steps
To a suspension of 0.30 g of tert-butyl (2,3-dihydro(1,4)dioxino(2,3-c)pyridin-7-ylmethyl)(1-(2-(7-fluoro-2-oxo-1,5-naphthyridin-1(2H)-yl)ethyl)piperidin-4-yl)carbamate in 2 mL of 2-propanol, 0.23 mL of concentrated hydrochloric acid was added, and the resultant mixture was stirred for 1 hour and 50 minutes under reflux with heating. The reaction mixture was cooled to 5° C., and the solid was obtained by filtration to give 0.28 g of 1-(2-(4-((2,3-dihydro(1,4)dioxino(2,3-c)pyridin-7-ylmethyl)amino)piperidin-1-yl)ethyl)-7-fluoro-1,5-naphthyridin-2(1H)-one trihydrochloride as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08354426B2 |
|---|
| Source dataset | uspto-grants-2013_01 |
|---|
| ORD ID | ord-6d42c3df329c44e6854d19bf4d15a39f |
|---|
| Source note | uspto-grants-2013_01 |
|---|