HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657069Generated: October 30, 2026
Hydrochloric Acid → HCID 25032630, compound
https://huagongshe.com/reaction/657069
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrafluoro-m-phenylenediamine dihydrochloride | HCID 149026 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 7-Chloro-3-oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazine-6-carbaldehyde | HCID 57486872 | — |
| Reactant | HCID 68991212 | HCID 68991212 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 25032630 | HCID 25032630 | — |
Reaction Steps
A solution of 1-{2-[(3S)-3-(aminomethyl)-1-piperidinyl]ethyl}-7-fluoro-2(1H)-quinolinone (90 mg; 0.3 mmol) and 7-chloro-3-oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazine-6-carboxaldehyde (for a synthesis see WO2003064421, Example 15(c)) (64 mg, 0.3 mmol) in methanol (2 ml), DCM (4 ml) was stirred at rt overnight. Sodium triacetoxyborohydride (0.127 g; 0.6 mmol) was added and the mixture was stirred at room temperature for 1 h. The reaction was evaporated and chromatographed on silica gel, eluting with 0-15% methanol-DCM-1% NH4OH to give an oil. The oil was treated with 1M HCl in Et2O to give the title compound (14 mg) as the dihydrochloride salt. 1H NMR (400 MHz, CD3OD) δ ppm 1.07 (s, 1H) 1.59-1.69 (m, 1H) 1.71-1.83 (m, 2H) 1.83-1.94 (m, 2H) 2.15-2.23 (m, 1H) 2.56-2.61 (m, 21H) 2.63-2.75 (m, 3H) 2.97 (s, 1H) 3.13-3.20 (m, 1H) 3.90 (s, 2H) 4.49 (td, J=14.21, 7.71 Hz, 2H) 6.67 (d, J=9.60 Hz, 1H) 7.11 (td, J=8.46, 2.27 Hz, 1H) 7.38-7.50 (m, 2H) 7.75 (dd, J=8.72, 6.19 Hz, 1H) 7.91 (d, J=9.60 Hz, 1H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08071592B2 |
|---|
| Source dataset | uspto-grants-2011_12 |
|---|
| ORD ID | ord-85ece8654bb4437187b1c3dd23b60796 |
|---|
| Source note | uspto-grants-2011_12 |
|---|