HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4-Dimethylbenzaldehyde → HCID 20817836, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4-Dimethylbenzaldehyde | HCID 22278 | — |
| Reactant | 6-Chloro-4-(piperidin-4-ylamino)chromen-2-one | HCID 11637695 | — |
| Product | HCID 20817836 | HCID 20817836 | — |
Reaction Steps
Prepared from 6-Chloro-4-(piperidin-4-ylamino)-chromen-2-one and 3,4-dimethyl benzaldehyde in a manner analogous to that described above. MS (ESI) m/e 397.1 (M+H)+. 1H NMR (500 MHz, MeOD-d4) δ ppm 8.12 (d, 1H), 7.60 (dd, 1H), 7.21-7.34 (m, 4H), 5.44 (s, 1H), 4.27 (s, 2H), 3.83-3.87 (m, 1H), 3.55-3.60 (m, 2H), 3.16-3.20 (m, 2H), 2.30-2.38 (m, 2H), 2.33 (s, 3H), 2.31 (s, 3H), 1.89-1.96 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06921821B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-fa37bf473ba44ca9bf14d8aae9a9b35f |
| Source note | uspto-grants-2005_07 |