HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598274Generated: October 30, 2026
Water → (7-Benzyloxy-3-nitroquinolin-4-yl)-(2-phenoxyethyl)amine
https://huagongshe.com/reaction/598274
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Phenoxyethanamine | HCID 15651 | — |
| Reactant | 7-(Benzyloxy)-4-chloro-3-nitroquinoline | HCID 21075751 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (7-Benzyloxy-3-nitroquinolin-4-yl)-(2-phenoxyethyl)amine | HCID 67050949 | 96.6% |
Reaction Steps
Triethylamine (8.93 mL, 64.1 mmol) was added to a solution of 7-benzyloxy-4-chloro-3-nitroquinoline (13.45 g, 42.7 mmol), prepared in Parts A-D of Example 1, in dichloromethane (250 mL). 2-Phenoxyethylamine (6.15 mL, 47.0 mmol) was added dropwise over a period of ten minutes, and the reaction mixture was stirred for three hours at ambient temperature. Distilled water (200 mL) was added to the solution, and the aqueous layer was washed with dichloromethane (2×200 mL). The combined organic solutions were dried over magnesium sulfate, filtered, and concentrated under reduced pressure to provide a solid. The solid was washed with hexanes, isolated by filtration, and dried under reduced pressure to provide 17.14 g of (7-benzyloxy-3-nitroquinolin-4-yl)-(2-phenoxyethyl)amine as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07897597B2 |
|---|
| Source dataset | uspto-grants-2011_03 |
|---|
| ORD ID | ord-4d6a72d3558344a0a99a0da18d9bc481 |
|---|
| Source note | uspto-grants-2011_03 |
|---|