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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992589Generated: October 30, 2026

Triethylamine → 3-[(3-Nitro[1,5]naphthyridin-4-yl)amino]propan-1-ol

https://huagongshe.com/reaction/1992589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Aminobutan-1-olHCID 12202791—
Reactant4-Chloro-3-nitro-1,5-naphthyridineHCID 13122787—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product3-[(3-Nitro[1,5]naphthyridin-4-yl)amino]propan-1-olHCID 6854043998%

Reaction Steps

To a solution of 4-chloro-3-nitro[1,5]naphthyridine (18.0 g, 85.9 mmol) in dichloromethane (220 mL) at room temperature was added triethylamine (15.6 mL, 112 mmol) and 3-amino-1-butanol (7.20 mL, 94.5 mmol). The solution was stirred for 4 hours and then was concentrated under reduced pressure to yield an orange solid. The solid was slurried in water (250 mL) for 30 minutes, isolated by filtration, washed with water (3×30 mL), and dried at 70° C. in a vacuum oven to afford 20.9 g of 3-[(3-nitro[1,5]naphthyridin-4-yl)amino]propan-1-ol as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07648997B2
Source datasetuspto-grants-2010_01
ORD IDord-a9f6cb9789d0424e8d656d863c1b4f5a
Source noteuspto-grants-2010_01