Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 46846505 | HCID 46846505 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 46909864 | HCID 46909864 | 142.2% |
Reaction Steps
4′-[(1R)-1-[[(6,7-dichloro-3-oxo-2,3-dihydro-4H-1,4-benzoxazin-4-yl)acetyl](methyl)amino]-2-(1-pyrrolidinyl)ethyl]-3-biphenylcarboxamide, Trifluoroacetate salt (94 mg, 0.135 mmol) was dissolved in 20 mL of ethyl acetate. A 1:1 mixture of saturated sodium bicarbonate and water was prepared separately, and 20 mL of this solution was delivered to the flask containing 4′-[(1R)-1-[[(6,7-dichloro-3-oxo-2,3-dihydro-4H-1,4-benzoxazin-4-yl)acetyl](methyl)amino]-2-(1-pyrrolidinyl)ethyl]-3-biphenylcarboxamide, Trifluoroacetate salt. This mixture was magnetically stirred for one hour at room temperature and then the mixture was diluted with 40 mL of ethyl acetate. The organic phase was separated from the aqueous phase, dried over magnesium sulfate, filtered, and concentrated under vacuum. The resulting free base material was taken up in 1 mL of dioxane and then 2 mL of a 4M HCl/dioxane solution was slowly added. A white solid precipitated out of solution and then the flask containing the mixture was transferred to a sonicator and was sonicated for 20 minutes. The mixture was transferred to a vial and dried under vacuum to give 4′-[(1R)-1-[[(6,7-dichloro-3-oxo-2,3-dihydro-4H-1,4-benzoxazin-4-yl)acetyl](methyl)amino]-2-(1-pyrrolidinyl)ethyl]-3-biphenylcarboxamide, Hydrochloride salt (59.3 mg, 0.096 mmol, 71%) as an off-white solid. MS (ES) m/e 583 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07749998B2 |
|---|
| Source dataset | uspto-grants-2010_07 |
|---|
| ORD ID | ord-4d0c730bb7f54ddcb3d174bec975b9c6 |
|---|
| Source note | uspto-grants-2010_07 |
|---|