HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 67547229, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 3-bromo-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one | HCID 291524 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 64122985 | HCID 64122985 | — |
| Product | HCID 67547229 | HCID 67547229 | — |
Reaction Steps
The title compound was prepared from 3-bromo-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one (1.2 g, 5.012 mmol) and (3-methoxy-2-propoxy)benzaldehyde (1.17 g, 6.021 mmol) in the presence of sodium ethoxide (0.512 g, 7.521 mmol) in absolute ethanol (25 ml) as described in Intermediate 1 to give 681 mg of the product as a light yellow solid; 1H NMR (300 MHz, CDCl3) δ 1.15 (t, J=7.8 Hz, 3H), 1.89 (q, J=7.2 Hz, 2H), 3.87 (s, 3H), 3.99 (t, J=6.6 Hz, 2H), 6.91 (d, J=7.5 Hz, 1H), 7.05-7.11 (m, 2H), 7.33 (d, J=7.2 Hz, 1H), 7.58-7.70 (m, 3H), 8.42 (d, J=13.8 Hz, 1H), 8.94 (d, J=6.9 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08349846B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-1dbb4f6545624b23bdda115ee598c1b7 |
| Source note | uspto-grants-2013_01 |