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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44754Generated: October 25, 2026

1,1,1-Trimethoxybutane → 4-[(2-propyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)methyl]tetrahydro-2H-pyran-4-ol

https://huagongshe.com/reaction/44754

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1,1-TrimethoxybutaneHCID 123512—
Reactant4-[(3-Amino[1,5]naphthyridin-4-ylamino)methyl]tetrahydropyran-4-olHCID 66919188—
CatalystPyridinium chlorideHCID 10176127—
SolventTolueneHCID 1140—
Product4-[(2-propyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)methyl]tetrahydro-2H-pyran-4-olHCID 5751545969.2%

Reaction Steps

Trimethylorthobutyrate (1.9 mL, 12.0 mmol) and pyridine hydrochloride (23 mg, 0.2 mmol) were added to a suspension of 4-[(3-amino[1,5]naphthyridin-4-ylamino)methyl]tetrahydropyran-4-ol (10.0 mmol) in toluene (50 mL). The reaction mixture was heated at reflux overnight and then concentrated under reduced pressure. The residue was triturated with acetonitrile and the resulting solid was isolated by filtration to provide 2.26 g of 4-[(2-propyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)methyl]tetrahydro-2H-pyran-4-ol as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541438B2
Source datasetuspto-grants-2013_09
ORD IDord-ee4d7896f3c94d31bfbdef497c42ae6c
Source noteuspto-grants-2013_09