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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187422Generated: November 1, 2026

Water → 3-[(7-Bromo-3-nitro[1,5]naphthyridin-4-yl)amino]propan-1-ol

https://huagongshe.com/reaction/1187422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant3-Amino-1-propanolHCID 9086—
Reactant7-Bromo-4-chloro-3-nitro[1,5]naphthyridineHCID 57457837—
SolventDichloromethaneHCID 6344—
Product3-[(7-Bromo-3-nitro[1,5]naphthyridin-4-yl)amino]propan-1-olHCID 6853460888.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 7-bromo-4-chloro-3-nitro[l,5]naphthyridine (22.53 g, 78.10 g) in dichloromethane (260 mL) at room temperature was added triethylamine (14.2 mL, 102 mmol). The solution was cooled to 0° C. and 3-amino-1-propanol (6.57 mL, 85.9 mmol) was added. The solution was stirred for 20 minutes at room temperature and then was concentrated under reduced pressure to yield a yellow solid. Water (250 mL) was added to the solid, and the mixture was sonicated for 10 minutes. The solid was isolated by filtration, washed with water, and dried at 70° C. under vacuum to afford 22.60 g of 3-[(7-bromo-3-nitro[1,5]naphthyridin-4-yl)amino]propan-1-ol as a yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673932B2
Source datasetuspto-grants-2014_03
ORD IDord-a151a453e2b3490bb1e7cf14b7d3f562
Source noteuspto-grants-2014_03