HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → N-(6-(7-azabicyclo[2.2.1]heptan-7-yl)-4-methylpyridin-3-yl)-5-methyl-4-oxo-1,4-dihydroquinoline-3-carboxamide hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | N-(6-(7-azabicyclo[2.2.1]heptan-7-yl)-4-methylpyridin-3-yl)-5-methyl-4-oxo-1,4-dihydroquinoline-3-carboxamide | HCID 45259022 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(6-(7-azabicyclo[2.2.1]heptan-7-yl)-4-methylpyridin-3-yl)-5-methyl-4-oxo-1,4-dihydroquinoline-3-carboxamide hydrochloride | HCID 67368807 | — |
Reaction Steps
N-(6-(7-azabicyclo[2.2.1]heptan-7-yl)-4-methylpyridin-3-yl)-5-methyl-4-oxo-1,4-dihydroquinoline-3-carboxamide was dissolved in methanol (2 mL) and treated with 2 M HCl in ether (295.3 μL of 2 M, 0.5906 mmol). The solution was evaporated to provide N-(6-(7-azabicyclo[2.2.1]heptan-7-yl)-4-methylpyridin-3-yl)-5-methyl-4-oxo-1,4-dihydroquinoline-3-carboxamide hydrochloride. 1H NMR (400.0 MHz, DMSO-d6) δ 12.71 (s, 1H), 12.12 (s, 1H), 8.78 (s, 1H), 8.74 (s, 1H), 7.63-7.59 (m, 1H), 7.54 (d, J=8.3 Hz, 1H), 7.22 (d, J=7.1 Hz, 1H), 6.81 (s, 1H), 4.44 (s, 2H), 2.91 (s, 3H), 2.28 (s, 3H), 1.65 (d, J=7.2 Hz, 4H), 1.42 (d, J=6.8 Hz, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08969382B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-d22b834923bf4b6bb566ab534af7abfe |
| Source note | uspto-grants-2015_03 |