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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989118Generated: October 30, 2026

Acetyl chloride → HCID 22172706, compound

https://huagongshe.com/reaction/989118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant2-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)ethaneamineHCID 21946027—
SolventDichloromethaneHCID 6344—
ProductHCID 22172706HCID 2217270687.5%

Reaction Steps

Under a nitrogen atmosphere, acetyl chloride (50 μL, 0.7 mmole) in dichloromethane (25 mL) was added dropwise to a cooled (ice bath) solution of 2-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)ethaneamine (0.2 g, 0.7 mmol) in dichloromethane (50 mL). After the addition was complete, the reaction mixture was allowed to warm to ambient temperature. After 30 minutes thin layer chromatography indicated that the reaction was complete. The reaction mixture was washed with 10% sodium hydroxide, water and brine; dried; and concentrated under vacuum to provide 0.25 g of crude product. This material was purified by column chromatography (silica gel eluting with dichloromethane) to provide 0.2 g of a solid. This solid was recrystallized from acetonitrile (30 mL) to provide 0.18 g of N′-[2-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)ethyl]acetamide as a white powder, m.p.228-230° C. Analysis: Calculated for C17H22N6O: %C, 62.56; %H, 6.79; %N, 25.75; Found: %C, 62.50; %H, 6.59; %N, 26.04. HRMS (EI) calcd for C22H26N6O2 (M+) 326.1855, found 326.1846

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06638944B2
Source datasetuspto-grants-2003_10
ORD IDord-a96b5819ae694d85a265f07505ccbc12
Source noteuspto-grants-2003_10