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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623096Generated: November 2, 2026

Acetic Acid → HCID 86612245, compound

https://huagongshe.com/reaction/1623096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 86612244HCID 86612244—
SolventMethanolHCID 887—
ProductHCID 86612245HCID 86612245106.8%

Reaction Steps

Sodium cyanoborohydride (0.54 g, 8.64 mmol, 3 eq) and acetic acid (7 mL) were added to a solution of 4-(4-amino-2-propyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)butyraldehyde O-methyloxime (0.94 g, 2.88 mmol, 1 eq) in methanol (7 mL) and stirred at ambient temperature for 20 minutes. The reaction mixture was concentrated under reduced pressure and diluted with dichloromethane (60 mL) and saturated aqueous sodium bicarbonate (40 mL). The phases were separated and the aqueous phase was adjusted to pH ˜8 with solid sodium bicarbonate and extracted with dichloromethane (2×20 mL). The combined organics were dried over magnesium sulfate, filtered, and then concentrated under reduced pressure to provide 1.01 g of 1-[4-(methoxyamino)butyl]-2-propyl-1H-imidazo[4,5-c]-1,5-naphthyridin-4-amine as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778963B2
Source datasetuspto-grants-2014_07
ORD IDord-2e58022b6cdc4931af8689e4b05feee5
Source noteuspto-grants-2014_07