HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinoline → HCID 11334324, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinoline | HCID 27833 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 3-Pyridinecarboxylic acid, 6-chloro-, 1-oxide | HCID 11457960 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 11334324 | HCID 11334324 | 35% |
Reaction Steps
6-Chloronicotinic acid 1-oxide (0.347 g, 2.0 mmol) and 2-ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline (0.544 g, 2.2 mmol) were mixed in chloroform (8 mL) at 0° C. 1-Methylpiperazine (0.30 g, 3.0 mmol) was added after 5 min and the reaction mixture was stirred for 16 h at room temperature. The solvent was removed in vacuo and the residual oil was purified on a silica gel column using chloroform/methanol/triethylamine, (100:20:1), as the eluent to give 0.18 g, (35% yield) of the title compound as a brownish solid: 1H NMR (DMSO-d6, 400 MHz) δ 8.56 (s, 1H), 7.90 (d, J=8.0 Hz, 1H), 7.39 (d, J=8.0 Hz, 1H), 3.63 (br s, 2H), 3.39 (br s, 2H), 2.43 (br s, 2H), 2.34 (br s, 2H), 2.25 (s, 3H); MS (EI) m/z 256 and 258 (M++1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07683067B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-71ca1e1c548d4bfcbcf029f3ef7a6577 |
| Source note | uspto-grants-2010_03 |