HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 10152749, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 22380830 | HCID 22380830 | — |
| Reactant | HCID 22380835 | HCID 22380835 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 10152749 | HCID 10152749 | — |
Reaction Steps
A mixture of 1-Methyl-1-o-tolyl-1,2,3,4-tetrahydro-isoquinoline (96 mg, 0.40 mmol), 2-chloro-N-(2-fluoro-benzyl)-N-indan-2-yl-acetamide (147 mg, 0.40 mmol), and potassium carbonate (111 mg, 0.80 mmol) in actonitrile (10 ml) is heated at reflux for 30 hours. The reaction mixture is cooled, treated with water, and extracted with ethyl acetate. The combined extracts are washed with brine, dried over sodium sulfate and concentrated in vacuo. The residue is purified by preparative thin layer chromatography to give 2-(1-Ethyl-1-o-tolyl-3,4-dihydro-1H-isoquinolin-2-yl)-N-(2-fluoro-benzyl)-N-indan-2-yl-acetamide (Compound 4) as a pale yellow oil. LSMS 519.3 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06916830B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-bc8780245d7a4e789a50a4fb22832f21 |
| Source note | uspto-grants-2005_07 |