HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3-{[6-(4-fluorophenyl)-2,3-dihydropyrido[3,2-f][1,4]oxazepin-4(5H)-yl]carbonyl}benzylamine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | tert-butyl 3-{[6-(4-fluorophenyl)-2,3-dihydropyrido[3,2-f][1,4]oxazepin-4(5H)-yl]carbonyl}benzylcarbamate | HCID 67180248 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-{[6-(4-fluorophenyl)-2,3-dihydropyrido[3,2-f][1,4]oxazepin-4(5H)-yl]carbonyl}benzylamine hydrochloride | HCID 67179670 | — |
Reaction Steps
To tert-butyl 3-{[6-(4-fluorophenyl)-2,3-dihydropyrido[3,2-f][1,4]oxazepin-4(5H)-yl]carbonyl}benzylcarbamate (0.32 g) obtained in Example 72C was added a 4N solution (10 ml) of hydrochloric acid in ethyl acetate, and the mixture was stirred at room temperature for 30 min. The reaction mixture was concentrated and the residue was dissolved in a small amount of isopropanol. Ethyl acetate was added and the resulting crystals were collected by filtration to give the title compound (0.25 g) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07625887B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-bcf9aef530d844edba30dcf9bb90bf8a |
| Source note | uspto-grants-2009_12 |