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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant2-PhenoxyethanamineHCID 15651—
Reactant7-(Benzyloxy)-4-chloro-3-nitroquinolineHCID 21075751—
SolventDichloromethaneHCID 6344—
Product(7-Benzyloxy-3-nitroquinolin-4-yl)-(2-phenoxyethyl)amineHCID 6705094996.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897597B2
Source datasetuspto-grants-2011_03
ORD IDord-4d6a72d3558344a0a99a0da18d9bc481
Source noteuspto-grants-2011_03