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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623100Generated: November 3, 2026

Valeryl chloride → HCID 57455389, compound

https://huagongshe.com/reaction/1623100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantValeryl chlorideHCID 61186—
ReactantPyridinium chlorideHCID 10176127—
ReactantHCID 57455388HCID 57455388—
SolventDichloromethaneHCID 6344—
ProductHCID 57455389HCID 5745538988.3%

Reaction Steps

Valeryl chloride (1.8 mL, 15.3 mmol, 1.1 eq) was added dropwise to a solution of ethyl 4-[(3-amino[1,5]naphthyridin-4-yl)amino]butyrate (3.8 g, 13.9 mmol, 1 eq) in dichloromethane (55 mL) and stirred for one hour. The reaction mixture was concentrated under reduced pressure and was dissolved in pyridine (55 mL). Pyridine hydrochloride (0.16 g, 1.39 mmol, 0.1 eq) was added and the reaction mixture was heated to reflux for 18 hours. The reaction mixture was concentrated under reduced pressure and diluted with dichloromethane (100 mL) and saturated aqueous sodium bicarbonate (75 mL). The phases were separated and the aqueous phase was extracted with dichloromethane (2×30 mL). The combined organics were dried over magnesium sulfate, stirred over decolorizing charcoal, filtered through CELITE filter aid, concentrated under reduced pressure, and dried at 35° C. under high vacuum to afford 4.18 g of ethyl 4-(2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)butyrate as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778963B2
Source datasetuspto-grants-2014_07
ORD IDord-43bb95a7806042d08e46a8bc309a4412
Source noteuspto-grants-2014_07