HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isobutylamine → 7-bromo-N-(2-methylpropyl)-3-nitro[1,5]naphthyridin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isobutylamine | HCID 6558 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 7-Bromo-4-chloro-3-nitro[1,5]naphthyridine | HCID 57457837 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-bromo-N-(2-methylpropyl)-3-nitro[1,5]naphthyridin-4-amine | HCID 67052211 | 98.3% |
Reaction Steps
Triethylamine (17.97 mL, 129.0 mmol) was added to a solution of 7-bromo-4-chloro-3-nitro[1,5]naphthyridine (24.8 g, 86.0 mmol) in dichloromethane (200 mL) at 0° C. Isobutylamine (9.40 mL, 94.6 mmol) was added dropwise to the mixture, and the mixture was stirred for 3 hours at ambient temperature. The reaction mixture was condensed under reduced pressure to a solid, which was triturated with water (200 mL). The precipitate was filtered, washed sequentially with water and hexanes, and dried to yield 27.5 g of 7-bromo-3-nitro[1,5]naphthyridin-4-yl-(2-methylpropyl)amine as a yellow powder, mp 114-115° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07897609B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-06659af59b464135a880d92ff7aeb186 |
| Source note | uspto-grants-2011_03 |