HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992613Generated: October 30, 2026
Water → 3-[(7-Bromo-3-nitro[1,5]naphthyridin-4-yl)amino]propan-1-ol
https://huagongshe.com/reaction/1992613
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Amino-1-propanol | HCID 9086 | — |
| Reactant | 7-Bromo-4-chloro-3-nitro[1,5]naphthyridine | HCID 57457837 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-[(7-Bromo-3-nitro[1,5]naphthyridin-4-yl)amino]propan-1-ol | HCID 68534608 | 88.5% |
Reaction Steps
To a solution of 7-bromo-4-chloro-3-nitro[1,5]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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07648997B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-579195332050461b8d161c5f88a8e92b |
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| Source note | uspto-grants-2010_01 |
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