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HRID 601307作成日:2026年10月25日

1-amino-3-[7-(benzyloxy)-1,1-dioxido-4H-1,2,4-benzothiadiazin-3-yl]-4-hydroxyquinolin-2(1H)-one → 3-[7-(benzyloxy)-1,1-dioxido-4H-1,2,4-benzothiadiazin-3-yl]-4-hydroxy-1-{[2-methylpropylidene]amino}quinolin-2(1H)-one

https://huagongshe.com/reaction/601307

反応式

関与物質

役割名称HCID仕込み量
反応物1-amino-3-[7-(benzyloxy)-1,1-dioxido-4H-1,2,4-benzothiadiazin-3-yl]-4-hydroxyquinolin-2(1H)-oneHCID 136358484—
溶媒DimethylacetamideHCID 31374—
生成物3-[7-(benzyloxy)-1,1-dioxido-4H-1,2,4-benzothiadiazin-3-yl]-4-hydroxy-1-{[2-methylpropylidene]amino}quinolin-2(1H)-oneHCID 136358487169.4%

反応条件

温度165 °C

反応手順

The product of Example 304F (0.150 g, 0.32 mmol) and isobutyrlaldehyde (0.44 mL, 4.84 mmol) in N,N-dimethylacetamide (1.5 mL) were reacted at 125° C. for 40 minutes in a microwave reactor in a sealed tube. The reaction was concentrated under a stream of nitrogen warmed through a manifold heated to 165° C. The resulting residue was triturated with diethyl ether and filtered to give the title compound (0.140 g, 84%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07902203B2
出典データセットuspto-grants-2011_03
ORD IDord-48361b71a4bb4ea29a612de9662818b7
出典メモuspto-grants-2011_03