HuagongsheHuagongshe Chemistry Print Report · For research reference only
Quinoline → HCID 10063683, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Quinoline | HCID 7047 | — |
| Reactant | Morpholine, 4-(chloroacetyl)- | HCID 74040 | — |
| Reactant | HCID 21892153 | HCID 21892153 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 10063683 | HCID 10063683 | 29% |
Reaction Steps
1-(2-Morpholin-4-yl-2-oxo-ethyl)-quinolinium chloride: A stirred solution of 2-chloro-1-morpholin-4-yl-ethanone (1.02 g, 6.23 mmol), quinoline (700 μL, 5.91 mmol) and acetonitrile (15.0 mL) was refluxed at 96° C. for 6 h under argon. The solution was equilibrated to room temperature and the precipitate was filtered on a Buchner funnel. The solid was dried in vacuo to yield 349 mg (29%) of the title compound. 1H NMR (DMSO-d6): 9.58 (d, J=6.0 Hz, 1H), 9.42 (d, J=8.1 Hz, 1H), 8.53 (d, J=7.8 Hz, 1H), 8.44 (d, J=9.0 Hz, 1H), 8.28 (m, 2H), 8.06 (t, J=7.8 Hz, 1H), 3.82 (t, J=4.2 Hz, 2H), 3.65 (m, 4H), 3.47 (t, J=4.8 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07135480B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-c0485ada04be448aad4abe687e6d7720 |
| Source note | uspto-grants-2006_11 |