HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-[(3-Nitro[1,5]naphthyridin-4-yl)amino]propan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Aminobutan-1-ol | HCID 12202791 | — |
| Reactant | 4-Chloro-3-nitro-1,5-naphthyridine | HCID 13122787 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-[(3-Nitro[1,5]naphthyridin-4-yl)amino]propan-1-ol | HCID 68540439 | 98% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07648997B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-a9f6cb9789d0424e8d656d863c1b4f5a |
| Source note | uspto-grants-2010_01 |