HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → N-(3-aminopropyl)-N-[1-(3-benzylquinolin-2-yl)-2-methylpropyl]-3-fluoro-4-methylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | N-[1-(3-benzylquinolin-2-yl)-2-methylpropyl]-3-fluoro-N-[3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)propyl]-4-methylbenzamide | HCID 59836196 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(3-aminopropyl)-N-[1-(3-benzylquinolin-2-yl)-2-methylpropyl]-3-fluoro-4-methylbenzamide | HCID 11525920 | 13.4% |
Reaction Steps
To a solution of N-[1-(3-benzylquinolin-2-yl)-2-methylpropyl]-3-fluoro-N-[3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)propyl]-4-methylbenzamide 19 (19 mg, 1 eq) in ethanol (1 ml), was added hydrazine (3 μl, 3 eq). The reaction was stirred at room temperature for 2 h then heated to 40° C. for another hour. The precipitate was filtered through a PTFE filter and washed with CH2Cl2. The filtrate was concentrated and purified by flash chromatography to yield 2 mg of N-(3-aminopropyl)-N-[1-(3-benzylquinolin-2-yl)-2-methylpropyl]-3-fluoro-4-methylbenzamide 2 as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07452996B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-38eac5a30e0c44f7a33f87cdda5192de |
| Source note | uspto-grants-2008_11 |