HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Quinolinecarboxaldehyde → HCID 12150181, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Quinolinecarboxaldehyde | HCID 83641 | — |
| Reactant | 1-(1,3-Benzodioxol-5-yl)-1-isopropylurea | HCID 100555 | — |
| Product | HCID 12150181 | HCID 12150181 | 14% |
Reaction Steps
This compound was synthesized from N-isopropyl-N-[3,4-(methylenedioxy)-phenyl]urea (308 mg) and 3-quinolinecarboxaldehyde (243 mg) by the procedure described in example 10 in 14% yield. mp: 202-205° C. 1H NMR (CDCl3): 8.89 (d, J=2.0, 1H), 8.11 (d, J=7.6, 1H), 8.05 (s, 1H), 7.80 (d, J=7.6, 1H), 7.74 (t, J=7.6, 1H), 7.58 (t, J=7.6, 1H), 6.72 (s, 1H), 6.41 (s, 1H), 5.94 (s, 1H), 5.92 (s, 1H), 5.52 (d, J=1.9, 1H), 5.25 (s, 1H), 4.42 (m, 1H), 1.57 (d, J=7.0, 3H), 1.56 (d, J=7.0, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07652006B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-f80be232c0e7477dad35b950b2b56f18 |
| Source note | uspto-grants-2010_01 |