HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Ethanediamine, N1,N1,N2-trimethyl- → HCID 59224344, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Ethanediamine, N1,N1,N2-trimethyl- | HCID 67338 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | HCID 16660652 | HCID 16660652 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59224344 | HCID 59224344 | 30% |
Reaction Steps
A mixture of 5-(5-fluoro-2-methylphenoxymethyl)-6-(4-hydroxy-2-methoxyphenyl)-2,2,4-trimethyl-1,2-dihydroquinoline (Reference Compound No. 3-1, 26.0 mg, 0.0600 mmol), 1,1′-carbonyldiimidazole (31.4 mg, 0.194 mmol) and 4-dimethylaminopyridine (1.1 mg, 0.0090 mmol) was dissolved in anhydrous tetrahydrofuran (0.6 mL), and then the mixture was stirred at room temperature for 1 hour. N,N,N′-trimethylethylenediamine (15 μL, 0.12 mmol) was added thereto, the mixture was stirred at room temperature for 1 hour, and then the mixture was purified by silica gel column chromatography (hexane-ethyl acetate) to give the titled compound (10.0 mg) as a colorless amorphous product. (Yield 30%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08440660B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-60b23a6a392c4060a4ce6c4698c0515d |
| Source note | uspto-grants-2013_05 |