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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497753Generated: October 31, 2026

Acetone → N-(2-Methylpropyl)-3-nitro-1,5-naphthyridin-4-amine

https://huagongshe.com/reaction/497753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantIsobutylamineHCID 6558—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 178526774HCID 178526774—
SolventDimethylformamideHCID 6228—
ProductN-(2-Methylpropyl)-3-nitro-1,5-naphthyridin-4-amineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06949646B2
Source datasetuspto-grants-2005_09
ORD IDord-6f312a0cc16a41859695e62aa814d3a7
Source noteuspto-grants-2005_09