Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 12083037 | HCID 12083037 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 12083038 | HCID 12083038 | 101.2% |
Reaction Steps
A 250 mL round bottom flask equipped with a condenser is charged with ethanol (150 mL), triethylamine (0.93 mL) and diethyl 2-(ethoxy(3-(morpholin-4-ylmethyl)-5,6,7,8-tetrahydroquinolin-8-yl)methyl)malonate (Preparation 17, 750 mg). The solution is heated to reflux. After 12 h, the mixture is concentrated to give a yellow solid, which is purified by flash chromatography (silica gel, 6% MeOH: methylene chloride) to give 603 mg of the title compound. Physical characteristics: 1H NMR (DMSO-d6): δ9.02, 8.04, 7.58, 4.24, 3.59, 3.57, 3.01, 2.88, 2.42, 1.89, 1.30; 13C NMR (DMSO-d6): δ165.3, 154.1, 141.6, 138.3, 134.4, 132.8, 126.9, 125.3, 110.0, 104.3, 66.1, 59.7, 59.1, 52.9, 29.2, 27.8, 20.7, 14.3; IR (KBr) 3079, 3037, 2958, 2931, 2913, 2850, 2828, 1731, 1679, 1647, 1628, 1600, 1509, 1462, 1450, 1297, 1270, 1251, 1227, 1206, 1114, 1097, 1079; HRMS m/z 357.1818.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06624159B2 |
|---|
| Source dataset | uspto-grants-2003_09 |
|---|
| ORD ID | ord-1c6f69a65e4f41029ddd11c5c8cda1af |
|---|
| Source note | uspto-grants-2003_09 |
|---|