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HRID 257053作成日:2026年10月27日

Cesium carbonate → 6-(2,2-Dimethoxyethoxy)-1-oxo-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/reaction/257053

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物Cesium iodideHCID 24601—
反応物2-Bromo-1,1-dimethoxyethaneHCID 81672—
反応物6-Hydroxy-1,2,3,4-tetrahydroisoquinolin-1-oneHCID 15908314—
溶媒DimethylformamideHCID 6228—
生成物6-(2,2-Dimethoxyethoxy)-1-oxo-1,2,3,4-tetrahydroisoquinolineHCID 18963883—

反応手順

6-Hydroxy-1-oxo-1,2,3,4-tetrahydroisoquinoline is treated with bromacetaldehyde dimethyl acetal, in the presence of Cs2CO3 and CsI in DMF to yield 6-(2,2-dimethoxyethoxy)-1-oxo-1,2,3,4-tetrahydroisoquinoline. Treatment with 2-chloromethylpyridine hydrochloride in the presence of sodium hydride in DMF yields 6-(2,2-dimethoxyethoxy)2-(2-pyridylmethyl)-1-oxo-1,2,3,4-tetrahydroisoquinoline. Hydrolysis with 20% aqueous sulfuric acid in THF yields α-[2-(2-pyridylmethyl)-1-oxo-1,2,3,4-tetrahydroisoquinolin-6-yloxy]-acetaldehyde which is then converted to 2-(2-pyridylmethyl)-6-[2-(N-hydroxyamino)-ethoxy]-1-oxo-1,2,3,4-tetrahydroisoquinoline.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05260316
出典データセットuspto-grants-1993_11
ORD IDord-ebf4cc4857a445ca810ceabd00a34116
出典メモuspto-grants-1993_11