HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N1-(3-nitro-7-phenylquinolin-4-yl)-2-methylpropane-1,2-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Methylpropylenediamine | HCID 13128 | — |
| Reactant | 4-Chloro-3-nitro-7-phenylquinoline | HCID 21984335 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N1-(3-nitro-7-phenylquinolin-4-yl)-2-methylpropane-1,2-diamine | HCID 86593761 | — |
Reaction Steps
A solution of 1,2-diamino-2-methylpropane (9.3 mL, 88.9 mmol) and triethylamine (5.0 mL, 35.5 mmol) in dichloromethane (100 mL) was cooled to 0° C. A solution of 4-chloro-3-nitro-7-phenylquinoline (5.06 g, 17.8 mmol) in dichloromethane (50 mL) was added over a period of 45 minutes, and then the reaction was allowed to warm to ambient temperature. The solution was washed sequentially with water (2×100 mL) and brine (150 mL), dried over sodium sulfate, filtered, and concentrated under reduced pressure to provide N1-(3-nitro-7-phenylquinolin-4-yl)-2-methylpropane-1,2-diamine as an orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07091214B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-488bb10254d64e94955ce5a59e9d54b2 |
| Source note | uspto-grants-2006_08 |