HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352483Generated: October 29, 2026
Acetone → N-(2-Methylpropyl)-3-nitro-1,5-naphthyridin-4-amine
https://huagongshe.com/reaction/352483
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetone | HCID 180 | — |
| Reactant | Isobutylamine | HCID 6558 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 178526774 | HCID 178526774 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(2-Methylpropyl)-3-nitro-1,5-naphthyridin-4-amine | HCID 54184816 | — |
Reaction Steps
Phosphorous oxychloride (0.6 mL, 6.44 mmol) was reacted with N,N-dimethylformamide then added to a solution of 3-nitro[1,5]naphthyridin-4-ol (1.0 g, 5.23 mmol) in N,N-dimethylformamide (20 mL). The reaction mixture was warmed using a jacketed flask with refluxing acetone as a heat source. After 3 hours the reaction mixture was poured into ice water, isobutylamine (2.0 mL, 20.1 mmol) was added and the mixture was heated on a steam bath. After several hours the reaction mixture was cooled to ambient temperature, filtered and washed with water. The aqueous layer was extracted with dichloromethane. The dichloromethane extract was washed with aqueous sodium bicarbonate, washed with water, dried over magnesium filtrate then loaded onto a layer of silica gel. The silica gel was eluted initially with dichloromethane to remove an impurity then with 5% methanol in dichloromethane to recover the product. The eluant was concentrated to dryness to provide N4-(2-methylpropyl)-3-nitro[1,5]naphthyridin-4-amine as a solid, m.p. 97-99° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06747040B2 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-ad8e5a3baea6499391f2c94c9786c885 |
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| Source note | uspto-grants-2004_06 |
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