HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Quinolinecarboxaldehyde → HCID 117732478, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Quinolinecarboxaldehyde | HCID 79619 | — |
| Reactant | HCID 117732476 | HCID 117732476 | — |
| Product | HCID 117732478 | HCID 117732478 | — |
Reaction Steps
Using the procedure described in Example 21, Step C, the title compound was prepared from Compound 23b and 2-quinolinecarbaldehyde. 1H-NMR (400 MHz, CDCl3) δ (ppm): 8.66 (d, J=2.2 Hz, 1H), 8.09 (d, J=8.3 Hz, 1H), 7.97-8.07 (m, 2H), 7.89 (d, J=5.6 Hz, 1H), 7.79 (d, J=8.1 Hz, 1H), 7.70 (ddd, J=8.4, 6.9, 1.3 Hz, 1H), 7.46-7.56 (m, 2H), 6.81 (d, J=9.0 Hz, 1H), 6.03 (d, J=5.6 Hz, 1H), 5.30 (t, J=5.3 Hz, 1H), 4.91 (d, J=5.4 Hz, 2H), 3.81 (s, 8H), 3.49-3.69 (m, 8H), 1.50 (s, 9H). Mass Spectrum (LCMS, ESI pos.) Calcd. For C34H39N9O3: 622.3 (M+H). Found: 622.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09193736B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-b6d1e0a0d9f4448eb998ae26e87076a0 |
| Source note | uspto-grants-2015_11 |