HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinoline → HCID 18430946, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinoline | HCID 27833 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 18430908 | HCID 18430908 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 18430946 | HCID 18430946 | — |
Reaction Steps
A mixture of 1-[2-(4-benzyl-1-piperazinyl)ethyl]cyclopentanecarboxylic acid (300 mg, 0.948 mmol), NH4HCO3 and 2-ethoxy-N-ethoxycarbonyl-1,2-dihydroquinoline (469 mg, 3.49 mmol) in chloroform (5.0 ml) was stirred for 2 d. To the mixture was added sat NaHCO3 (3 ml) and the mixture was extracted with dichloromethane After the solvent was removed in vacuo, the residue was extracted with dichloromethane (30 ml). The extract was washed with brine, dried over Na2SO4, filtered and concentrated in vacuo . The residue was purified by column chromatography (SiO2, 200-350 mesh/21 g/dichloromethane:methanol=97:3) to provide a yellow oil (174 mg/58%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06444677B2 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-390e6a38a6aa4448a7b8e4d35fcf23e8 |
| Source note | uspto-grants-2002_09 |