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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598007Generated: October 26, 2026

Isobutylamine → 7-bromo-N-(2-methylpropyl)-3-nitro[1,5]naphthyridin-4-amine

https://huagongshe.com/reaction/598007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutylamineHCID 6558—
ReactantTriethylamineHCID 8471—
Reactant7-Bromo-4-chloro-3-nitro[1,5]naphthyridineHCID 57457837—
SolventDichloromethaneHCID 6344—
Product7-bromo-N-(2-methylpropyl)-3-nitro[1,5]naphthyridin-4-amineHCID 6705221198.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897609B2
Source datasetuspto-grants-2011_03
ORD IDord-06659af59b464135a880d92ff7aeb186
Source noteuspto-grants-2011_03