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HRID 44754作成日:2026年10月25日

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

反応式

関与物質

役割名称HCID仕込み量
反応物1,1,1-TrimethoxybutaneHCID 123512—
反応物4-[(3-Amino[1,5]naphthyridin-4-ylamino)methyl]tetrahydropyran-4-olHCID 66919188—
触媒Pyridinium chlorideHCID 10176127—
溶媒TolueneHCID 1140—
生成物4-[(2-propyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)methyl]tetrahydro-2H-pyran-4-olHCID 5751545969.2%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541438B2
出典データセットuspto-grants-2013_09
ORD IDord-ee4d7896f3c94d31bfbdef497c42ae6c
出典メモuspto-grants-2013_09