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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366636Generated: November 1, 2026

Water → HCID 68874499, compound

https://huagongshe.com/reaction/2366636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium DithioniteHCID 24489—
ReactantHCID 68873567HCID 68873567—
Catalyst1,1'-Diethyl-4,4'-bipyridinium dibromideHCID 11474262—
SolventDichloromethaneHCID 6344—
ProductHCID 68874499HCID 68874499—

Reaction Steps

Ethyl N-(3-nitroquinolin-4-yl)-β-alaninate (62.0 g, 214 mmol, prepared as described in Part A of Example 15) was treated with sodium hydrosulfite (130.6 g, 750.1 mmol), potassium carbonate (117 g, 847 mmol), and ethyl viologen dibromide (0.802 g, 2.14 mmol) according to a modification of the method described in Part A of Example 8. After the reaction was stirred overnight, additional water (100 mL), dichloromethane, and sodium hydrosulfite (20.0 g, 115 mmol) were added, and the reaction was stirred for three additional hours. The organic layer was separated; washed with water (6×), saturated aqueous sodium bicarbonate, and brine; dried over magnesium sulfate; filtered; and concentrated under reduced pressure to provide 40.2 g of ethyl N-(3-aminoquinolin-4-yl)-β-alaninate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697873B2
Source datasetuspto-grants-2014_04
ORD IDord-9dc6ce1a239343ca94f922e8563efc6a
Source noteuspto-grants-2014_04