HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Ethyl 3-[(3-nitroquinolin-4-yl)amino]butanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl 3-aminobutyrate | HCID 98103 | — |
| Reactant | 4-Chloro-3-nitroquinoline | HCID 11275808 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 3-[(3-nitroquinolin-4-yl)amino]butanoate | HCID 67157227 | 99.8% |
Reaction Steps
Triethylamine (12.8 mL, 91.8 mmol) was added to a solution of 4-chloro-3-nitroquinoline (8.0 g, 38 mmol) in DMF (100 mL). The resulting solution was stirred for five minutes at room temperature, and then ethyl 3-aminobutyrate (6.2 mL, 42 mmol) was added. The reaction was stirred overnight at room temperature and poured into deionized water (320 mL). The mixture was extracted with ethyl acetate (1×125 mL and 2×100 mL). The combined extracts were washed with brine (3×120 mL), dried over magnesium sulfate, filtered through a layer of CELITE filter agent, concentrated under reduced pressure, and further dried under high vacuum to provide 11.5 g of ethyl 3-[(3-nitroquinolin-4-yl)amino]butanoate as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08207162B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-778c59d0d2c54868bf75267799273d1b |
| Source note | uspto-grants-2012_06 |