HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2E)-3-(4-Chlorophenyl)acryloyl chloride → (2E)-3-(4-chlorophenyl)-N-(2-piperidin-1-ylquinolin-6-yl)prop-2-enamide hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2E)-3-(4-Chlorophenyl)acryloyl chloride | HCID 11252649 | — |
| Reactant | Quinoline-2,6-diamine | HCID 22018948 | — |
| Reactant | 2-Piperidin-1-ylquinolin-6-amine | HCID 22018974 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (2E)-3-(4-chlorophenyl)-N-(2-piperidin-1-ylquinolin-6-yl)prop-2-enamide hydrochloride | HCID 22018962 | — |
Reaction Steps
To a solution of the product of Step D (91 mg, 0.4 mmol) in 2 mL HOAc was added the product of Step E (64 mg, 0.32 mmol). The resulting mixture was stirred at r.t. for 3 h then diluted with 3 mL ether. The resulting mixture was filtered and the resulting solids were washed with ether. The solids were dried under vacuum to afford the product, MS: m/z 392 (MH+), as an off-white solid. Using the appropriate starting materials and following procedures similar to those described above for Example 1, the following compounds were prepared from the corresponding quinoline-2,6-diamine intermediates:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07084156B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-7ea16d5540f64108a374fefb1059f324 |
| Source note | uspto-grants-2006_08 |